{{Rsnum
|rsid=556621
|Chromosome=6
|position=44626422
|Orientation=minus
|GMAF=0.3182
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 8.8 | 41.6 | 49.6
| HCB | 27.0 | 49.6 | 23.4
| JPT | 31.0 | 48.7 | 20.4
| YRI | 0.7 | 10.9 | 88.4
| ASW | 0.0 | 15.8 | 84.2
| CHB | 27.0 | 49.6 | 23.4
| CHD | 28.7 | 47.2 | 24.1
| GIH | 6.9 | 48.5 | 44.6
| LWK | 1.8 | 14.5 | 83.6
| MEX | 19.0 | 44.8 | 36.2
| MKK | 0.6 | 20.5 | 78.8
| TSI | 10.8 | 34.3 | 54.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22941190
  |Trait=Stroke (ischemic)
  |Title=Common variants at 6p21.1 are associated with large artery atherosclerotic stroke.
  |RiskAllele=A
  |Pval=5E-8
  |OR=1.21
  |ORtxt=[1.13-1.30]
  |OA=1
}}

{{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}}