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Variant : CV535441 (Single allele) Homo sapiens

Symbol: CV535441
Name: Single allele
Condition: Schizophrenia [RCV000754161]
Clinical Significance: pathogenic
Last Evaluated: 03/20/2018
Review Status: criteria provided, single submitter
Related Genes: ARHGAP11B   CHRFAM7A   CHRNA7   FAN1   GOLGA8H   GOLGA8Q   GOLGA8R   KLF13   LINC02352   MIR211   MTMR10   OTUD7A   TRPM1  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: research
Position
Human AssemblyChrPosition (strand)Source
GRCh381530,325,774 - 32,194,551CLINVAR
Cytogenetic Map1515q13.2-13.3CLINVAR
Trait Synonyms: SCHIZOPHRENIA WITH OR WITHOUT AN AFFECTIVE DISORDER



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14352146
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-10-08
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.