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rs6646773

From SNPedia

Orientationplus
Stabilizedplus
Make rs6646773(A;A)
Make rs6646773(A;G)
Make rs6646773(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position117088295
is asnp
is mentioned by
dbSNPrs6646773
ebirs6646773
HLIrs6646773
Exacrs6646773
Varsomers6646773
Maprs6646773
PheGenIrs6646773
hapmaprs6646773
1000 genomesrs6646773
hgdprs6646773
ensemblrs6646773
gopubmedrs6646773
geneviewrs6646773
scholarrs6646773
googlers6646773
pharmgkbrs6646773
gwascentralrs6646773
openSNPrs6646773
23andMers6646773
23andMe allrs6646773
SNP Nexus

SNPshotrs6646773
SNPdbers6646773
MSV3drs6646773
GWAS Ctlgrs6646773
GMAF0.1608
Max Magnitude
? (A;A) (A;G) (G;G) 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 C
P-val 1E-6
Odds Ratio NR NR