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rs10174573

From SNPedia

Orientationplus
Stabilizedplus
Make rs10174573(C;C)
Make rs10174573(C;T)
Make rs10174573(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position192877447
is asnp
is mentioned by
dbSNPrs10174573
ebirs10174573
HLIrs10174573
Exacrs10174573
Varsomers10174573
Maprs10174573
PheGenIrs10174573
hapmaprs10174573
1000 genomesrs10174573
hgdprs10174573
ensemblrs10174573
gopubmedrs10174573
geneviewrs10174573
scholarrs10174573
googlers10174573
pharmgkbrs10174573
gwascentralrs10174573
openSNPrs10174573
23andMers10174573
23andMe allrs10174573
SNP Nexus

SNPshotrs10174573
SNPdbers10174573
MSV3drs10174573
GWAS Ctlgrs10174573
GMAF0.4591
Max Magnitude
? (C;C) (C;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 2E-6
Odds Ratio 1.56 [1.39-1.74]