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rs17710780

From SNPedia

Orientationplus
Stabilizedplus
Make rs17710780(C;C)
Make rs17710780(C;T)
Make rs17710780(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position149657413
is asnp
is mentioned by
dbSNPrs17710780
dbSNP (classic)rs17710780
ClinGenrs17710780
ebirs17710780
HLIrs17710780
Exacrs17710780
Gnomadrs17710780
Varsomers17710780
LitVarrs17710780
Maprs17710780
PheGenIrs17710780
Biobankrs17710780
1000 genomesrs17710780
hgdprs17710780
ensemblrs17710780
geneviewrs17710780
scholarrs17710780
googlers17710780
pharmgkbrs17710780
gwascentralrs17710780
openSNPrs17710780
23andMers17710780
SNPshotrs17710780
SNPdbers17710780
MSV3drs17710780
GWAS Ctlgrs17710780
GMAF0.09688
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23377640OA-icon.png]
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 T
P-val 4E-6
Odds Ratio 1.66 [1.45-1.88]