{{Rsnum
|rsid=7018475
|Chromosome=9
|position=22137686
|Orientation=plus
|GMAF=0.2984
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 6.2 | 41.6 | 52.2
| HCB | 14.6 | 44.5 | 40.9
| JPT | 19.5 | 45.1 | 35.4
| YRI | 4.1 | 35.4 | 60.5
| ASW | 10.5 | 36.8 | 52.6
| CHB | 14.6 | 44.5 | 40.9
| CHD | 10.2 | 52.8 | 37.0
| GIH | 12.0 | 51.0 | 37.0
| LWK | 4.5 | 31.8 | 63.6
| MEX | 24.1 | 43.1 | 32.8
| MKK | 3.2 | 33.3 | 63.5
| TSI | 9.8 | 37.3 | 52.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22293688
|Trait=None
|Title=1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data.
|RiskAllele=
|Pval=3E-8
|OR=1.3500
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}