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Variant : CV535505 (Single allele) Homo sapiens

Symbol: CV535505
Name: Single allele
Condition: Schizophrenia [RCV000754225]
Clinical Significance: likely pathogenic
Last Evaluated: 03/20/2018
Review Status: criteria provided, single submitter
Related Genes: DDX1   E2F6   GACAT3   GREB1   LINC00276   LINC00570   LINC01804   LPIN1   LRATD1   MIR3125   MIR3681   MIR3681HG   MIR4262   MIR4429   MIR548S   MYCN   MYCNOS   MYCNUT   NBAS   NTSR2   ROCK2   SLC66A3   TRIB2  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: research
Position
Human AssemblyChrPosition (strand)Source
GRCh38211,177,745 - 16,113,827CLINVAR
Cytogenetic Map22p25.1-24.3CLINVAR
Trait Synonyms: SCHIZOPHRENIA WITH OR WITHOUT AN AFFECTIVE DISORDER



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14352263
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-12-03
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.