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Variant : CV535446 (Single allele) Homo sapiens

Symbol: CV535446
Name: Single allele
Condition: Schizophrenia [RCV000754166]
Clinical Significance: likely pathogenic
Last Evaluated: 03/20/2018
Review Status: criteria provided, single submitter
Related Genes: AC010931.1   AC113208.4   ADPGK   ADPGK-AS1   ARID3B   BBS4   C15orf39   CCDC33   CD276   CLK3   COX5A   CPLX3   CSK   CYP11A1   CYP1A1   CYP1A2   EDC3   FAM219B   GOLGA6A   GOLGA6B   GOLGA6C   HCN4   HIGD2B   INSYN1   INSYN1-AS1   ISLR   ISLR2   LINC02255   LMAN1L   LOXL1   LOXL1-AS1   MIR12135   MIR4513   MIR6881   MIR6882   MPI   NEO1   NPTN   NPTN-IT1   PML   PPCDC   REC114   RPP25   SCAMP2   SCAMP5   SEMA7A   STOML1   STRA6   TBC1D21   UBL7   UBL7-AS1   ULK3  
Variant Type: duplication (SO:1000035)
Source: CLINVAR
Evidence: research
Position
Human AssemblyChrPosition (strand)Source
GRCh381572,640,623 - 75,277,317CLINVAR
Cytogenetic Map1515q24.1-24.2CLINVAR
Trait Synonyms: SCHIZOPHRENIA WITH OR WITHOUT AN AFFECTIVE DISORDER



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14352155
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-08-04
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.