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rs4663476

From SNPedia

Orientationplus
Stabilizedplus
Make rs4663476(G;G)
Make rs4663476(G;T)
Make rs4663476(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position234692420
is asnp
is mentioned by
dbSNPrs4663476
ebirs4663476
HLIrs4663476
Exacrs4663476
Varsomers4663476
Maprs4663476
PheGenIrs4663476
hapmaprs4663476
1000 genomesrs4663476
hgdprs4663476
ensemblrs4663476
gopubmedrs4663476
geneviewrs4663476
scholarrs4663476
googlers4663476
pharmgkbrs4663476
gwascentralrs4663476
openSNPrs4663476
23andMers4663476
23andMe allrs4663476
SNP Nexus

SNPshotrs4663476
SNPdbers4663476
MSV3drs4663476
GWAS Ctlgrs4663476
GMAF0.1947
Max Magnitude
? (G;G) (G;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 G
P-val 0.000008
Odds Ratio 1.2300 None