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Variant : CV535563 (Single allele) Homo sapiens

Symbol: CV535563
Name: Single allele
Condition: Autistic disorder of childhood onset [RCV000754283]
Clinical Significance: likely pathogenic
Last Evaluated: 03/20/2018
Review Status: criteria provided, single submitter
Related Genes: CHL1   CHL1-AS1   CHL1-AS2   CNTN4   CNTN4-AS2   CNTN6   LINC01266  
Variant Type: duplication (SO:1000035)
Source: CLINVAR
Evidence: research
Position
Human AssemblyChrPosition (strand)Source
GRCh38354,166 - 2,405,982CLINVAR
Cytogenetic Map33p26.3CLINVAR
Trait Synonyms: Autism



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14351935
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-02-20
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.