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rs1525293

From SNPedia

Orientationplus
Stabilizedplus
Make rs1525293(C;C)
Make rs1525293(C;T)
Make rs1525293(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position71008019
is asnp
is mentioned by
dbSNPrs1525293
dbSNP (classic)rs1525293
ClinGenrs1525293
ebirs1525293
HLIrs1525293
Exacrs1525293
Gnomadrs1525293
Varsomers1525293
LitVarrs1525293
Maprs1525293
PheGenIrs1525293
Biobankrs1525293
1000 genomesrs1525293
hgdprs1525293
ensemblrs1525293
geneviewrs1525293
scholarrs1525293
googlers1525293
pharmgkbrs1525293
gwascentralrs1525293
openSNPrs1525293
23andMers1525293
SNPshotrs1525293
SNPdbers1525293
MSV3drs1525293
GWAS Ctlgrs1525293
GMAF0.3453
Max Magnitude0
? (C;C) (C;T) (T;T) 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 2E-6
Odds Ratio 1.70 [1.48-1.92]