{{Rsnum
|rsid=12449964
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|position=17641390
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 20.4 | 55.8 | 23.9
| HCB | 84.7 | 13.9 | 1.5
| JPT | 79.6 | 18.6 | 1.8
| YRI | 67.3 | 31.3 | 1.4
| ASW | 59.6 | 33.3 | 7.0
| CHB | 84.7 | 13.9 | 1.5
| CHD | 79.8 | 19.3 | 0.9
| GIH | 55.4 | 38.6 | 5.9
| LWK | 58.2 | 37.3 | 4.5
| MEX | 41.4 | 44.8 | 13.8
| MKK | 51.9 | 44.2 | 3.8
| TSI | 35.3 | 46.1 | 18.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=24262325
  |Trait=Coronary artery disease or ischemic stroke
  |Title=Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
  |RiskAllele=
  |Pval=2E-8
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}