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rs10065906

From SNPedia

Orientationplus
Stabilizedplus
Make rs10065906(A;A)
Make rs10065906(A;C)
Make rs10065906(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position159580770
is asnp
is mentioned by
dbSNPrs10065906
ebirs10065906
HLIrs10065906
Exacrs10065906
Varsomers10065906
Maprs10065906
PheGenIrs10065906
hapmaprs10065906
1000 genomesrs10065906
hgdprs10065906
ensemblrs10065906
gopubmedrs10065906
geneviewrs10065906
scholarrs10065906
googlers10065906
pharmgkbrs10065906
gwascentralrs10065906
openSNPrs10065906
23andMers10065906
23andMe allrs10065906
SNP Nexus

SNPshotrs10065906
SNPdbers10065906
MSV3drs10065906
GWAS Ctlgrs10065906
GMAF0.2723
Max Magnitude
? (A;A) (A;C) (C;C) 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 C
P-val 2E-6
Odds Ratio 1.17 [1.11-1.22]