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GENE - TERM ANNOTATION REPORT

178 Annotations Found.

An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • Curation Notes: ClinVar Annotator: match by term: Arrhythmogenic right ventricular cardiomyopathy, type 10


  • An association has been curated linking DSG2-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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-AS1 and arrhythmogenic right ventricular dysplasia 10 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for 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)
  • 2 papers in CRRD have been used to annotate DSG2-AS1
  • 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


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.