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rs1706631

From SNPedia

Orientationminus
Stabilizedminus
Make rs1706631(A;A)
Make rs1706631(A;T)
Make rs1706631(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position17509301
is asnp
is mentioned by
dbSNPrs1706631
ebirs1706631
HLIrs1706631
Exacrs1706631
Varsomers1706631
Maprs1706631
PheGenIrs1706631
hapmaprs1706631
1000 genomesrs1706631
hgdprs1706631
ensemblrs1706631
gopubmedrs1706631
geneviewrs1706631
scholarrs1706631
googlers1706631
pharmgkbrs1706631
gwascentralrs1706631
openSNPrs1706631
23andMers1706631
23andMe allrs1706631
SNP Nexus

SNPshotrs1706631
SNPdbers1706631
MSV3drs1706631
GWAS Ctlgrs1706631
GMAF0.455
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 23377640]
Trait Major depressive disorder
Title Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.
Risk Allele T
P-val 6E-6
Odds Ratio 1.35 [1.22-1.49]