{{Rsnum
|rsid=17019682
|Chromosome=12
|position=91911494
|Orientation=plus
|GMAF=0.06566
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 86.7 | 13.3 | 0.0
| HCB | 97.1 | 2.9 | 0.0
| JPT | 98.2 | 1.8 | 0.0
| YRI | 71.9 | 24.7 | 3.4
| ASW | 75.4 | 22.8 | 1.8
| CHB | 97.1 | 2.9 | 0.0
| CHD | 99.1 | 0.9 | 0.0
| GIH | 67.3 | 28.7 | 4.0
| LWK | 75.5 | 22.7 | 1.8
| MEX | 89.7 | 10.3 | 0.0
| MKK | 89.1 | 10.3 | 0.6
| TSI | 84.2 | 14.9 | 1.0
| 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=0.000002
|OR=1.47
|ORtxt=[0.98-2.22]
|OA=1
}}

{{on chip | Affy GenomeWide 6}}