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rs6563353

From SNPedia

Orientationplus
Stabilizedplus
Make rs6563353(C;C)
Make rs6563353(C;T)
Make rs6563353(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position83556097
is asnp
is mentioned by
dbSNPrs6563353
ebirs6563353
HLIrs6563353
Exacrs6563353
Varsomers6563353
Maprs6563353
PheGenIrs6563353
hapmaprs6563353
1000 genomesrs6563353
hgdprs6563353
ensemblrs6563353
gopubmedrs6563353
geneviewrs6563353
scholarrs6563353
googlers6563353
pharmgkbrs6563353
gwascentralrs6563353
openSNPrs6563353
23andMers6563353
23andMe allrs6563353
SNP Nexus

SNPshotrs6563353
SNPdbers6563353
MSV3drs6563353
GWAS Ctlgrs6563353
GMAF0.1511
Max Magnitude
? (C;C) (C;T) (T;T) 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 A
P-val 2E-6
Odds Ratio NR NR