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rs2509382

From SNPedia

Orientationplus
Stabilizedplus
Make rs2509382(C;C)
Make rs2509382(C;G)
Make rs2509382(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position91046275
is asnp
is mentioned by
dbSNPrs2509382
ebirs2509382
HLIrs2509382
Exacrs2509382
Varsomers2509382
Maprs2509382
PheGenIrs2509382
hapmaprs2509382
1000 genomesrs2509382
hgdprs2509382
ensemblrs2509382
gopubmedrs2509382
geneviewrs2509382
scholarrs2509382
googlers2509382
pharmgkbrs2509382
gwascentralrs2509382
openSNPrs2509382
23andMers2509382
23andMe allrs2509382
SNP Nexus

SNPshotrs2509382
SNPdbers2509382
MSV3drs2509382
GWAS Ctlgrs2509382
GMAF0.1437
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 22891933] Analysis of the DISC1 translocation partner (11q14.3) in genetic risk of schizophrenia


[PMID 25670952OA-icon.png] Disrupted-in-Schizophrenia-1 SNPs and Susceptibility to Schizophrenia: Evidence from Malaysia