{{Rsnum
|rsid=2046383
|Chromosome=12
|position=29951209
|Orientation=plus
|GMAF=0.2948
|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 | 4.4 | 33.6 | 61.9
| HCB | 8.8 | 47.4 | 43.8
| JPT | 15.9 | 48.7 | 35.4
| YRI | 11.6 | 40.8 | 47.6
| ASW | 7.0 | 45.6 | 47.4
| CHB | 8.8 | 47.4 | 43.8
| CHD | 10.1 | 49.5 | 40.4
| GIH | 12.9 | 51.5 | 35.6
| LWK | 11.0 | 45.9 | 43.1
| MEX | 10.3 | 24.1 | 65.5
| MKK | 9.6 | 46.2 | 44.2
| TSI | 8.8 | 46.1 | 45.1
| 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=1.39
|ORtxt=[0.97-1.97]
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}