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rs1457614

From SNPedia

Orientationplus
Stabilizedplus
Make rs1457614(A;A)
Make rs1457614(A;C)
Make rs1457614(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position13488772
is asnp
is mentioned by
dbSNPrs1457614
dbSNP (classic)rs1457614
ClinGenrs1457614
ebirs1457614
HLIrs1457614
Exacrs1457614
Gnomadrs1457614
Varsomers1457614
LitVarrs1457614
Maprs1457614
PheGenIrs1457614
Biobankrs1457614
1000 genomesrs1457614
hgdprs1457614
ensemblrs1457614
geneviewrs1457614
scholarrs1457614
googlers1457614
pharmgkbrs1457614
gwascentralrs1457614
openSNPrs1457614
23andMers1457614
SNPshotrs1457614
SNPdbers1457614
MSV3drs1457614
GWAS Ctlgrs1457614
GMAF0.2608
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GWAS snp
PMID [PMID 23377640OA-icon.png]
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 C
P-val 8E-6
Odds Ratio 1.47 [1.29-1.64]