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GENE - TERM ANNOTATION REPORT

406 Annotations Found.

An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13466879 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13499646 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11653128 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607129 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10046296 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:23861362, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:34899054 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612574 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607119 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:23861362, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38481306 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054904 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15135588 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12900965 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14692408 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12889421 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38467393 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26921841 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38484174 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11628709 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38459736 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569382 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:23861362, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15106270 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12889765 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:34895868 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569379 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:17105751, PMID:20031616, PMID:20129281, PMID:20829228, PMID:21606390, PMID:21606396, PMID:21636032, PMID:21723241, PMID:21859740, PMID:23071725, PMID:23812740, PMID:23861362, PMID:24033266, PMID:24070718, PMID:24436435, PMID:25637381, PMID:25741868, PMID:26138720, PMID:26899768, PMID:28492532, PMID:29062102


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607130 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:20400443, PMID:23861362, PMID:24070718, PMID:25741868, PMID:28492532, PMID:28600387


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569381 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:23861362, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569383 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:21075724 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532, PMID:29247119


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569380 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:23861362, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15167974 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26893899 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38462491 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26884682 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15143211 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26913974 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8690914 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:21397041, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691563 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:25637381, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9690136 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:21606396, PMID:23861362, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26896585 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:20400443, PMID:23071725, PMID:24585727, PMID:27532257, PMID:28492532, PMID:29178656, PMID:30790397


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13499375 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12902399 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26916643 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10449807 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:21606396, PMID:24704780, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607132 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:17105751, PMID:18382419, PMID:18678517, PMID:19039334, PMID:19569224, PMID:20031616, PMID:20603720, PMID:20857253, PMID:21397041, PMID:21606390, PMID:21606396, PMID:23299917, PMID:23671136, PMID:23861362, PMID:24033266, PMID:24055113, PMID:24082139, PMID:24704780, PMID:25332820, PMID:25445213, PMID:25637381, PMID:25741868, PMID:26230511, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607116 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607117 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:23861362, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12843572 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607120 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:16025435, PMID:17105751, PMID:18382419, PMID:18678517, PMID:19039334, PMID:19863551, PMID:20864495, PMID:23299917, PMID:23861362, PMID:24033266, PMID:24503780, PMID:25087486, PMID:25172079, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:34896955 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26904963 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9693490 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:23861362, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607135 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26891044 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607107 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607141 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607111 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13467725 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607121 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38499514 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26888901 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:19151369, PMID:28472724, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26895805 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:23381804, PMID:23911551, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12835779 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607118 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607125 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11544617 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689980 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607126 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13464930 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607110 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11545696 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607122 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:20716751, PMID:23861362, PMID:24033266, PMID:24503780, PMID:25741868, PMID:27114410, PMID:27532257, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26913632 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11093456 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:24033266, PMID:24125834, PMID:25741868, PMID:27005929, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13542072 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688451 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26888363 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11617557 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26923538 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9693601 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:17372169, PMID:23861362, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:34888954 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054918 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26905697 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26902846 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:20864495, PMID:21397041, PMID:23381804, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26920231 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26923007 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11632834 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:27532257, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054922 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:17105751, PMID:19279339, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11547599 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13497940 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13500836 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13468096 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13501115 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13477150 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8565844 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:16505173


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607099 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:18632414, PMID:23514727, PMID:24033266, PMID:24238504, PMID:25741868, PMID:25765472, PMID:28492532, PMID:28578331, PMID:30454721


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38458676 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9687740 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:21606390, PMID:23299917, PMID:23861362, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8565843 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:16773573, PMID:18382419, PMID:20031617, PMID:20708101, PMID:20857253, PMID:23299917, PMID:24033266, PMID:24055113, PMID:25213555, PMID:25637381, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607104 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11090130 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607106 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8565842 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:16773573, PMID:20031617, PMID:20152563, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38476603 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8565840 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:16773573


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612557 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13500085 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8565845 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:16505173, PMID:24070718, PMID:25741868, PMID:28471438, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12881229 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13499246 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:34892072 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13466149 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38490825 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12890377 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38498326 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13498010 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10042621 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:26822237


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13468587 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38490306 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612550 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612565 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12891909 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26886798 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12899944 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532, PMID:30311386


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38480417 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26901926 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12884857 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054900 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38488601 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26916736 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38495472 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13534162 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:20400443, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054901 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:16505173, PMID:23071725, PMID:24033266, PMID:24070718, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38485765 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:34898288 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10041721 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26902384 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38481355 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38482299 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11614269 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13705637 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607096 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:20031617, PMID:20152563, PMID:20864495, PMID:21606390, PMID:21606396, PMID:21636032, PMID:21859740, PMID:23299917, PMID:23381804, PMID:23810894, PMID:23861362, PMID:23871674, PMID:23871885, PMID:23889974, PMID:24033266, PMID:24503780, PMID:24704780, PMID:25445213, PMID:25741868, PMID:26230511, PMID:27194543, PMID:27930701, PMID:28255936, PMID:28341588, PMID:28492532, PMID:28818065, PMID:30311386, PMID:30790397


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38491264 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612704 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612540 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612692 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054927 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:25741868, PMID:28492532, PMID:30985088


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054908 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612543 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612536 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12882956 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691562 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612699 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10041719 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24125834, PMID:25741868, PMID:27055156, PMID:28492532, PMID:30311386


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13521450 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612598 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612582 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607137 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:22214898, PMID:24033266, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612554 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38466529 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12892265 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612579 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38493800 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14723953 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:17105751, PMID:19151369, PMID:20829228, PMID:28492532, PMID:30311386


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13809920 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13813735 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10046299 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:20031617, PMID:23861362, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13816726 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8565846 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:16505173, PMID:23381804, PMID:23911551, PMID:24033266, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13809792 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:23381804, PMID:23911551, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13820701 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13803920 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13820654 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:20864495, PMID:21397041, PMID:23381804, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13809793 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:20864495, PMID:21397041, PMID:23381804, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13818700 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8565839 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:16773573, PMID:19151369, PMID:19863551, PMID:20031617, PMID:20152563, PMID:20400443, PMID:20857253, PMID:23671136, PMID:24033266, PMID:25741868, PMID:25820315, PMID:28283360


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054899 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:20864495, PMID:21397041, PMID:23381804, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13806689 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28898736 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13814484 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38489937 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13802195 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13816930 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:20864495, PMID:21397041, PMID:23381804, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688450 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13815310 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607131 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:18639457, PMID:20031616, PMID:24033266, PMID:25741868, PMID:28492532, PMID:28600387


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627011 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11090589 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532, PMID:29178656


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607134 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:2040044, PMID:20400443, PMID:20857253, PMID:23381804, PMID:23671136, PMID:23810894, PMID:23889974, PMID:23911551, PMID:24033266, PMID:25525159, PMID:25820315, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10045131 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:23396983, PMID:25351510, PMID:25741868, PMID:26112015, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054919 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:21606390, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8569384 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:20829228, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11525733 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:20152563, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688414 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:20197793, PMID:23299917, PMID:24033266, PMID:24070718, PMID:25637381, PMID:25741868, PMID:27930701, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12900674 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38472513 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:20864495, PMID:21397041, PMID:23381804, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9832325 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607128 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:24033266, PMID:25741868


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607109 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:16025435, PMID:16774985, PMID:18382419, PMID:18678517, PMID:18813333, PMID:19039334, PMID:19863551, PMID:20031616, PMID:20031617, PMID:20829228, PMID:23861362, PMID:24033266, PMID:25741868


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14709217 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12884631 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14715065 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12900850 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607142 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:24033266, PMID:25741868


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12849507 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:20864495, PMID:21397041, PMID:23381804, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14704155 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13500412 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689237 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:24070718, PMID:25741868, PMID:26656175, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14724821 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14713054 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11628048 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607097 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607143 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:21606396, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14734099 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054920 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14716376 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14714377 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14718944 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054916 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14710586 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13465218 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:21606396, PMID:22000064, PMID:22214898, PMID:25741868, PMID:25820315, PMID:27532257, PMID:28492532, PMID:29178656, PMID:30311386, PMID:30454721


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691570 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14720651 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14709699 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13820702 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14708651 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:23381804, PMID:23911551, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14692184 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14735603 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10046294 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:23861362, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054907 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11096421 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12901954 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14703896 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:21606390, PMID:22036071, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11614165 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11613038 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607102 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:21636032, PMID:23861362, PMID:24033266, PMID:25741868, PMID:26230511, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28907493 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607114 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:23861362, PMID:24033266, PMID:25741868


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691567 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:21220045, PMID:23861362, PMID:24033266, PMID:25213555, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28901434 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607144 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:23861362, PMID:24033266, PMID:25741868


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607115 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:24033266, PMID:25741868


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11613945 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626916 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11619492 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11618523 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28898293 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28900827 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11613755 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11549065 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28907495 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11616751 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11645530 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11644932 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11612875 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11620560 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626562 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11621596 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11629217 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11651563 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12901747 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9690423 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28903357 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11614703 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11649208 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11658742 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11618511 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11616232 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11620638 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11040072 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:21606396, PMID:25741868


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11658460 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8565847 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:17105751, PMID:18678517, PMID:19039334, PMID:20031616, PMID:20031617, PMID:20716751, PMID:20864495, PMID:21606390, PMID:23810883, PMID:23861362, PMID:24033266, PMID:24055113, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28907352 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11629690 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28903541 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28902921 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10046298 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:23861362, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626690 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11613312 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11653204 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627694 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28901430 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11650660 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11651818 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28894256 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627713 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11648125 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627151 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11648044 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28907793 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28907796 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11652756 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28897993 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28901437 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28907795 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28900565 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688452 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:25741868


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11616991 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28900569 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28903182 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11618483 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28903724 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28903538 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28894253 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28898297 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:20400443


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11630645 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11651875 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11655194 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11629860 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691566 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054915 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:20708101, PMID:25213555, PMID:25741868, PMID:26633542, PMID:27532257, PMID:28454995, PMID:28492532, PMID:28567303, PMID:30615648


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13528152 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12887409 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612591 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13465763 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14736661 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11092492 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:25877686, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691564 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:20400443, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11040309 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13536119 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14728315 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26894631 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607136 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:23396983, PMID:24033266, PMID:24503780, PMID:25351510, PMID:25741868, PMID:27532257, PMID:28492532, PMID:30885746


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607139 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:21606390, PMID:23299917, PMID:24033266, PMID:25059832, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28901042 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12901636 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26906950 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12886441 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11524007 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:25741868, PMID:28492532, PMID:29178656, PMID:30993396


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26907148 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12902172 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11655173 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26899073 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12842199 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13466058 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28416588, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11542869 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:22458570, PMID:24033266, PMID:25741868, PMID:26656175, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26905197 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607103 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:21636032, PMID:23861362, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13807980 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13467793 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14394124 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25174650, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14394125 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10042620 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:23381804, PMID:23911551, PMID:25741868, PMID:27532257, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26920711 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9690405 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689236 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8690912 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8690913 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12892760 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14742731 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054892 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054902 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:20031616, PMID:20857253, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9586827 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11615031 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13815024 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054911 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532, PMID:29773157


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11628285 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12899344 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12888304 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11619798 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28898082 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607105 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12841347 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15101885 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11543042 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13501332 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12891872 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607112 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26885388 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12846497 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13486149 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9691569 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14701678 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15162268 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13538675 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:15116718 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14728321 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627473 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13526944 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12834189 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12834019 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607100 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:24033266, PMID:25741868


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11523748 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13612551 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13466018 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13466564 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13806070 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532, PMID:30533233


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13803041 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26917191 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12845016 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13529733 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054903 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:21606396, PMID:21636032, PMID:23178689, PMID:23889974, PMID:25741868, PMID:25820315, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054917 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:23514727, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13803812 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:20864495, PMID:21397041, PMID:23381804, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054926 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8690908 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12906354 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11628542 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054895 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10054930 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626519 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607095 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:21606390, PMID:24033266, PMID:24503780, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9693484 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:20031617, PMID:24033266, PMID:25741868, PMID:28492532


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8607127 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:21636032, PMID:21859740, PMID:24033266, PMID:25741868, PMID:28492532, PMID:29802319


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:39457081 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10
  • Original References(s): PMID:25741868


  • An association has been curated linking DSG2 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8565841 (Homo sapiens)
  • 3 CRRD objects have been annotated to arrhythmogenic right ventricular dysplasia 10  (DOID:0110081)
  • 6 papers in CRRD have been used to annotate DSG2
  • Curation Notes: ClinVar Annotator: match by term: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
  • Original References(s): PMID:16773573, PMID:20031616, PMID:20031617, PMID:20400443, PMID:20857253, PMID:21606390, PMID:21606396, PMID:23071725, PMID:23381804, PMID:24033266, PMID:25741868


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.