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rs4491175

From SNPedia

Orientationplus
Stabilizedplus
Make rs4491175(C;C)
Make rs4491175(C;T)
Make rs4491175(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position91223046
is asnp
is mentioned by
dbSNPrs4491175
ebirs4491175
HLIrs4491175
Exacrs4491175
Varsomers4491175
Maprs4491175
PheGenIrs4491175
hapmaprs4491175
1000 genomesrs4491175
hgdprs4491175
ensemblrs4491175
gopubmedrs4491175
geneviewrs4491175
scholarrs4491175
googlers4491175
pharmgkbrs4491175
gwascentralrs4491175
openSNPrs4491175
23andMers4491175
23andMe allrs4491175
SNP Nexus

SNPshotrs4491175
SNPdbers4491175
MSV3drs4491175
GWAS Ctlgrs4491175
GMAF0.4954
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22566498OA-icon.png]
Trait
Title Genomic association analysis identifies multiple loci influencing antihypertensive response to an angiotensin II receptor blocker.
Risk Allele T
P-val 0.000008
Odds Ratio 1.1000 None