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Variant : CV224846 (Single allele) Homo sapiens

Symbol: CV224846
Name: Single allele
Condition: Autism spectrum disorder [RCV000208724]|Autism spectrum disorders [RCV000208724]
Clinical Significance: uncertain significance
Last Evaluated: 08/12/2011
Review Status: no assertion criteria provided
Related Genes: LIMS3   LINC01123   MALL   MIR4267   MIR4436B1   MIR4436B2   MTLN   NPHP1   RANBP2   RGPD5  
Variant Type: duplication (SO:1000035)
Source: CLINVAR
Evidence: research
Position
Human AssemblyChrPosition (strand)Source
GRCh382109,696,399 - 110,327,308CLINVAR
GRCh372110,453,976 - 111,084,885CLINVAR
Cytogenetic Map22q13CLINVAR
Trait Synonyms: Autism spectrum disorders; Autism susceptibility; Epilepsy; Seizure Disorders



Disease Annotations
References - curated
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11050287
Created: 2016-04-12
Species: Homo sapiens
Last Modified: 2020-03-24
Status: ACTIVE



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