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rs11773966

From SNPedia

Orientationplus
Stabilizedplus
Make rs11773966(A;A)
Make rs11773966(A;C)
Make rs11773966(C;C)
ReferenceGRCh38 38.1/141
Chromosome8
Position53642640
is asnp
is mentioned by
dbSNPrs11773966
dbSNP (classic)rs11773966
ClinGenrs11773966
ebirs11773966
HLIrs11773966
Exacrs11773966
Gnomadrs11773966
Varsomers11773966
LitVarrs11773966
Maprs11773966
PheGenIrs11773966
Biobankrs11773966
1000 genomesrs11773966
hgdprs11773966
ensemblrs11773966
geneviewrs11773966
scholarrs11773966
googlers11773966
pharmgkbrs11773966
gwascentralrs11773966
openSNPrs11773966
23andMers11773966
SNPshotrs11773966
SNPdbers11773966
MSV3drs11773966
GWAS Ctlgrs11773966
GMAF0.01102
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GWAS snp
PMID [PMID 23092984OA-icon.png]
Trait Bipolar disorder (mood-incongruent)
Title Genome-wide association of mood-incongruent psychotic bipolar disorder.
Risk Allele A
P-val 2E-6
Odds Ratio 2.17 [NR]