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rs17766217

From SNPedia

Orientationplus
Stabilizedplus
Make rs17766217(C;C)
Make rs17766217(C;T)
Make rs17766217(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position127492252
is asnp
is mentioned by
dbSNPrs17766217
ebirs17766217
HLIrs17766217
Exacrs17766217
Varsomers17766217
Maprs17766217
PheGenIrs17766217
hapmaprs17766217
1000 genomesrs17766217
hgdprs17766217
ensemblrs17766217
gopubmedrs17766217
geneviewrs17766217
scholarrs17766217
googlers17766217
pharmgkbrs17766217
gwascentralrs17766217
openSNPrs17766217
23andMers17766217
23andMe allrs17766217
SNP Nexus

SNPshotrs17766217
SNPdbers17766217
MSV3drs17766217
GWAS Ctlgrs17766217
GMAF0.337
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 A
P-val 3E-7
Odds Ratio None None