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rs16965962

From SNPedia

Orientationplus
Stabilizedplus
Make rs16965962(A;A)
Make rs16965962(A;C)
Make rs16965962(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position105154672
is asnp
is mentioned by
dbSNPrs16965962
ebirs16965962
HLIrs16965962
Exacrs16965962
Varsomers16965962
Maprs16965962
PheGenIrs16965962
hapmaprs16965962
1000 genomesrs16965962
hgdprs16965962
ensemblrs16965962
gopubmedrs16965962
geneviewrs16965962
scholarrs16965962
googlers16965962
pharmgkbrs16965962
gwascentralrs16965962
openSNPrs16965962
23andMers16965962
23andMe allrs16965962
SNP Nexus

SNPshotrs16965962
SNPdbers16965962
MSV3drs16965962
GWAS Ctlgrs16965962
GMAF0.04729
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 22760553OA-icon.png]
Trait Response to citalopram treatment
Title Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.
Risk Allele T
P-val 3E-7
Odds Ratio NR NR