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rs7779057

From SNPedia

Orientationplus
Stabilizedplus
Make rs7779057(C;C)
Make rs7779057(C;T)
Make rs7779057(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position106954440
is asnp
is mentioned by
dbSNPrs7779057
dbSNP (classic)rs7779057
ClinGenrs7779057
ebirs7779057
HLIrs7779057
Exacrs7779057
Gnomadrs7779057
Varsomers7779057
LitVarrs7779057
Maprs7779057
PheGenIrs7779057
Biobankrs7779057
1000 genomesrs7779057
hgdprs7779057
ensemblrs7779057
geneviewrs7779057
scholarrs7779057
googlers7779057
pharmgkbrs7779057
gwascentralrs7779057
openSNPrs7779057
23andMers7779057
SNPshotrs7779057
SNPdbers7779057
MSV3drs7779057
GWAS Ctlgrs7779057
GMAF0.2103
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23151678]
Trait Serum tamsulosin hydrochloride concentration
Title Impact of four loci on serum tamsulosin hydrochloride concentration.
Risk Allele C
P-val 2E-7
Odds Ratio 17.16 [10.93-23.39] unit increase