Have questions? Visit https://www.reddit.com/r/SNPedia

rs491376

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs491376(C;G)
Make rs491376(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position13115138
is asnp
is mentioned by
dbSNPrs491376
ebirs491376
HLIrs491376
Exacrs491376
Varsomers491376
Maprs491376
PheGenIrs491376
hapmaprs491376
1000 genomesrs491376
hgdprs491376
ensemblrs491376
gopubmedrs491376
geneviewrs491376
scholarrs491376
googlers491376
pharmgkbrs491376
gwascentralrs491376
openSNPrs491376
23andMers491376
23andMe allrs491376
SNP Nexus

SNPshotrs491376
SNPdbers491376
MSV3drs491376
GWAS Ctlgrs491376
GMAF0.01331
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 22041458OA-icon.png]
Trait
Title Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.
Risk Allele C
P-val 0.000002
Odds Ratio None None