{{Rsnum
|rsid=10812610
|Chromosome=9
|position=27533986
|Orientation=plus
|GMAF=0.4807
|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 | 30.4 | 45.5 | 24.1
| HCB | 36.6 | 50.0 | 13.4
| JPT | 45.1 | 45.1 | 9.7
| YRI | 7.6 | 30.3 | 62.1
| ASW | 10.5 | 40.4 | 49.1
| CHB | 36.6 | 50.0 | 13.4
| CHD | 27.1 | 49.5 | 23.4
| GIH | 35.6 | 42.6 | 21.8
| LWK | 2.8 | 37.4 | 59.8
| MEX | 24.1 | 39.7 | 36.2
| MKK | 1.9 | 39.7 | 58.3
| TSI | 21.6 | 58.8 | 19.6
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20445134
|Trait=Heart failure
|Title=The Association of Genome-Wide Variation with the Risk of Incident Heart Failure in Adults of European and African Ancestry: A Prospective Meta-Analysis from the CHARGE Consortium
|RiskAllele=
|Pval=0.000005
|OR=1.14
|ORtxt=[0.99-1.31]
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}