{{Rsnum
|rsid=7043482
|Chromosome=9
|position=82521000
|Orientation=plus
|GMAF=0.4573
|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 | 48.7 | 35.4 | 15.9
| HCB | 11.7 | 40.9 | 47.4
| JPT | 5.3 | 49.6 | 45.1
| YRI | 1.4 | 26.5 | 72.1
| ASW | 3.5 | 43.9 | 52.6
| CHB | 11.7 | 40.9 | 47.4
| CHD | 11.9 | 46.8 | 41.3
| GIH | 59.4 | 34.7 | 5.9
| LWK | 4.5 | 26.4 | 69.1
| MEX | 41.4 | 44.8 | 13.8
| MKK | 5.1 | 32.1 | 62.8
| TSI | 43.1 | 47.1 | 9.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21901158
|Trait=None
|Title=Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study.
|RiskAllele=G
|Pval=0.000003
|OR=12.0000
|ORtxt=[7.00 - 18.00] % increase
|OA=1
}}

{{PMID Auto
|PMID=17434096
|Title=A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}