{{Rsnum
|rsid=6473383
|Chromosome=8
|position=82756885
|Orientation=plus
|GMAF=0.1501
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 1.8 | 31.0 | 67.3
| HCB | 0.0 | 2.3 | 97.7
| JPT | 0.0 | 0.9 | 99.1
| YRI | 13.2 | 57.6 | 29.2
| ASW | 8.8 | 49.1 | 42.1
| CHB | 0.0 | 2.3 | 97.7
| CHD | 0.0 | 3.8 | 96.2
| GIH | 6.9 | 36.6 | 56.4
| LWK | 9.2 | 36.7 | 54.1
| MEX | 1.8 | 10.7 | 87.5
| MKK | 12.8 | 52.6 | 34.6
| TSI | 5.0 | 23.0 | 72.0
| 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=0.000003
|OR=1.19
|ORtxt=[0.99-1.44]
|OA=1
}}

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