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rs882632

From SNPedia

Orientationminus
Stabilizedminus
Make rs882632(A;A)
Make rs882632(A;G)
Make rs882632(G;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position29057895
is asnp
is mentioned by
dbSNPrs882632
dbSNP (classic)rs882632
ClinGenrs882632
ebirs882632
HLIrs882632
Exacrs882632
Gnomadrs882632
Varsomers882632
LitVarrs882632
Maprs882632
PheGenIrs882632
Biobankrs882632
1000 genomesrs882632
hgdprs882632
ensemblrs882632
geneviewrs882632
scholarrs882632
googlers882632
pharmgkbrs882632
gwascentralrs882632
openSNPrs882632
23andMers882632
SNPshotrs882632
SNPdbers882632
MSV3drs882632
GWAS Ctlgrs882632
GMAF0.129
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 20125088OA-icon.png]
Trait Major depressive disorder
Title Genome-wide association study of recurrent early-onset major depressive disorder
Risk Allele T
P-val 0.000002
Odds Ratio 1.34 None