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rs11752643

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs11752643(C;T)
Make rs11752643(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32701596
is asnp
is mentioned by
dbSNPrs11752643
ebirs11752643
HLIrs11752643
Exacrs11752643
Varsomers11752643
Maprs11752643
PheGenIrs11752643
hapmaprs11752643
1000 genomesrs11752643
hgdprs11752643
ensemblrs11752643
gopubmedrs11752643
geneviewrs11752643
scholarrs11752643
googlers11752643
pharmgkbrs11752643
gwascentralrs11752643
openSNPrs11752643
23andMers11752643
23andMe allrs11752643
SNP Nexus

SNPshotrs11752643
SNPdbers11752643
MSV3drs11752643
GWAS Ctlgrs11752643
GMAF0.02112
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21971053OA-icon.png]
Trait
Title Genome-wide association study of coronary artery disease in the Japanese.
Risk Allele T
P-val 5E-7
Odds Ratio 1.2600 [1.15-1.38]