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rs9326246

From SNPedia

Orientationplus
Stabilizedplus
Make rs9326246(C;C)
Make rs9326246(C;G)
Make rs9326246(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position116741017
is asnp
is mentioned by
dbSNPrs9326246
ebirs9326246
HLIrs9326246
Exacrs9326246
Varsomers9326246
Maprs9326246
PheGenIrs9326246
hapmaprs9326246
1000 genomesrs9326246
hgdprs9326246
ensemblrs9326246
gopubmedrs9326246
geneviewrs9326246
scholarrs9326246
googlers9326246
pharmgkbrs9326246
gwascentralrs9326246
openSNPrs9326246
23andMers9326246
23andMe allrs9326246
SNP Nexus

SNPshotrs9326246
SNPdbers9326246
MSV3drs9326246
GWAS Ctlgrs9326246
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 23202125OA-icon.png] Large-scale association analysis identifies new risk loci for coronary artery disease.
GWAS snp
PMID [PMID 24262325OA-icon.png]
Trait Coronary artery disease
Title Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Risk Allele C
P-val 3E-7
Odds Ratio 1.15 [1.09-1.21]