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rs16902947

From SNPedia

Orientationplus
Stabilizedplus
Make rs16902947(A;A)
Make rs16902947(A;G)
Make rs16902947(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position36308995
is asnp
is mentioned by
dbSNPrs16902947
ebirs16902947
HLIrs16902947
Exacrs16902947
Varsomers16902947
Maprs16902947
PheGenIrs16902947
hapmaprs16902947
1000 genomesrs16902947
hgdprs16902947
ensemblrs16902947
gopubmedrs16902947
geneviewrs16902947
scholarrs16902947
googlers16902947
pharmgkbrs16902947
gwascentralrs16902947
openSNPrs16902947
23andMers16902947
23andMe allrs16902947
SNP Nexus

SNPshotrs16902947
SNPdbers16902947
MSV3drs16902947
GWAS Ctlgrs16902947
GMAF0.1667
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23151678]
Trait Serum tamsulosin hydrochloride concentration
Title Impact of four loci on serum tamsulosin hydrochloride concentration.
Risk Allele A
P-val 1E-7
Odds Ratio 19.48 [12.54-26.42] unit increase