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rs974379

From SNPedia

Orientationplus
Stabilizedplus
Make rs974379(A;A)
Make rs974379(A;C)
Make rs974379(C;C)
ReferenceGRCh38 38.1/141
Chromosome15
Position33212866
is asnp
is mentioned by
dbSNPrs974379
dbSNP (classic)rs974379
ClinGenrs974379
ebirs974379
HLIrs974379
Exacrs974379
Gnomadrs974379
Varsomers974379
LitVarrs974379
Maprs974379
PheGenIrs974379
Biobankrs974379
1000 genomesrs974379
hgdprs974379
ensemblrs974379
geneviewrs974379
scholarrs974379
googlers974379
pharmgkbrs974379
gwascentralrs974379
openSNPrs974379
23andMers974379
SNPshotrs974379
SNPdbers974379
MSV3drs974379
GWAS Ctlgrs974379
GMAF0.2231
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 1.29 [1.17-1.4]