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rs6724422

From SNPedia

Orientationplus
Stabilizedplus
Make rs6724422(C;C)
Make rs6724422(C;T)
Make rs6724422(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position67749656
is asnp
is mentioned by
dbSNPrs6724422
ebirs6724422
HLIrs6724422
Exacrs6724422
Varsomers6724422
Maprs6724422
PheGenIrs6724422
hapmaprs6724422
1000 genomesrs6724422
hgdprs6724422
ensemblrs6724422
gopubmedrs6724422
geneviewrs6724422
scholarrs6724422
googlers6724422
pharmgkbrs6724422
gwascentralrs6724422
openSNPrs6724422
23andMers6724422
23andMe allrs6724422
SNP Nexus

SNPshotrs6724422
SNPdbers6724422
MSV3drs6724422
GWAS Ctlgrs6724422
GMAF0.05372
Max Magnitude
? (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 T
P-val 4E-7
Odds Ratio None None