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Variant : CV535554 (Single allele) Homo sapiens

Symbol: CV535554
Name: Single allele
Condition: Schizophrenia [RCV000754274]
Clinical Significance: likely pathogenic
Last Evaluated: 03/20/2018
Review Status: criteria provided, single submitter
Related Genes: ATP13A4   ATP13A4-AS1   ATP13A5   ATP13A5-AS1   BCL6   CCDC50   CLDN1   CLDN16   FGF12   FGF12-AS1   FGF12-AS2   FGF12-AS3   FLJ42393   GMNC   HES1   IL1RAP   LINC00887   LINC01991   LINC02013   LINC02026   LINC02028   LINC02036   LINC02037   LINC02038   LINC02041   LINC02048   LPP   LPP-AS1   LPP-AS2   MASP1   MB21D2   MIR28   MIR944   OPA1   OPA1-AS1   OSTN   OSTN-AS1   P3H2   P3H2-AS1   PLAAT1   PYDC2   RTP2   RTP4   SNAR-I   SST   TMEM207   TP63   TPRG1   TPRG1-AS1   TPRG1-AS2   UTS2B  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: research
Position
Human AssemblyChrPosition (strand)Source
GRCh383187,222,939 - 194,312,782CLINVAR
Cytogenetic Map33q27.3-29CLINVAR
Trait Synonyms: SCHIZOPHRENIA WITH OR WITHOUT AN AFFECTIVE DISORDER



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14351925
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-11-12
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.