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rs573332

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs573332(C;C)
Make rs573332(C;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position13120911
is asnp
is mentioned by
dbSNPrs573332
ebirs573332
HLIrs573332
Exacrs573332
Varsomers573332
Maprs573332
PheGenIrs573332
hapmaprs573332
1000 genomesrs573332
hgdprs573332
ensemblrs573332
gopubmedrs573332
geneviewrs573332
scholarrs573332
googlers573332
pharmgkbrs573332
gwascentralrs573332
openSNPrs573332
23andMers573332
23andMe allrs573332
SNP Nexus

SNPshotrs573332
SNPdbers573332
MSV3drs573332
GWAS Ctlgrs573332
GMAF0.01331
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22041458OA-icon.png]
Trait
Title Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.
Risk Allele G
P-val 0.000001
Odds Ratio None None