{{Rsnum
|rsid=7173743
|Chromosome=15
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|position=78849442
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 20.0 | 50.8 | 29.2
| HCB | 26.7 | 44.4 | 28.9
| JPT | 20.0 | 40.0 | 40.0
| YRI | 25.4 | 45.8 | 28.8
| ASW | 20.4 | 53.7 | 25.9
| CHB | 26.7 | 44.4 | 28.9
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 17.1 | 48.0 | 34.9
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

{{PMID Auto
|PMID=3679547
|Title=Large-scale association analysis identifies new risk loci for coronary artery disease.
}}

{{PMID Auto GWAS
  |PMID=24262325
  |Trait=Coronary artery disease
  |Title=Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
  |RiskAllele=C
  |Pval=7E-8
  |OR=1.08
  |ORtxt=[1.05-1.11]
  }}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}