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Variant : CV237926 (Single allele) Homo sapiens

Symbol: CV237926
Name: Single allele
Condition: Autism spectrum disorder [RCV000225663]|Autism spectrum disorders [RCV000225663]
Clinical Significance: pathogenic
Last Evaluated: 10/12/2015
Review Status: criteria provided, single submitter
Related Genes: ATP10A   CYFIP1   GOLGA6L1   GOLGA6L2   GOLGA6L6   IPW   MAGEL2   MKRN3   NDN   NIPA1   NIPA2   NPAP1   OR4M2   OR4N4   POTEB   POTEB2   PWAR1   PWAR4   PWAR5   PWAR6   PWARSN   PWRN1   PWRN2   SNORD115-1   SNORD116-1   SNRPN   SNURF   TUBGCP5   UBE3A  
Variant Type: duplication (SO:1000035)
Source: CLINVAR
Evidence: research
Position
Human AssemblyChrPosition (strand)Source
GRCh371520,306,549 - 26,208,861CLINVAR
Cytogenetic Map1515q11.1-12CLINVAR
Trait Synonyms: ASD; autism; Autism spectrum disorders; Autism susceptibility



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 11345487
Created: 2016-07-12
Species: Homo sapiens
Last Modified: 2019-10-01
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.