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rs2314398

From SNPedia

Orientationplus
Stabilizedplus
Make rs2314398(C;C)
Make rs2314398(C;G)
Make rs2314398(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position96747751
is asnp
is mentioned by
dbSNPrs2314398
dbSNP (classic)rs2314398
ClinGenrs2314398
ebirs2314398
HLIrs2314398
Exacrs2314398
Gnomadrs2314398
Varsomers2314398
LitVarrs2314398
Maprs2314398
PheGenIrs2314398
Biobankrs2314398
1000 genomesrs2314398
hgdprs2314398
ensemblrs2314398
geneviewrs2314398
scholarrs2314398
googlers2314398
pharmgkbrs2314398
gwascentralrs2314398
openSNPrs2314398
23andMers2314398
SNPshotrs2314398
SNPdbers2314398
MSV3drs2314398
GWAS Ctlgrs2314398
GMAF0.2603
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GWAS
SNP rs2314398
PubMedID [PMID 18711365OA-icon.png]
Condition Bipolar disorder
Gene Intergenic
Risk Allele
pValue 3.00E-006
OR 1.17
95% CI




[PMID 25124521] Replication of previous genome-wide association studies of psychiatric diseases in a large schizophrenia case-control sample from Spain