{{Rsnum
|rsid=11172782
|Chromosome=12
|position=58865846
|Orientation=plus
|GMAF=0.1244
|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 | 95.3 | 4.7 | 0.0
| HCB | 71.1 | 28.9 | 0.0
| JPT | 80.7 | 19.3 | 0.0
| YRI | 42.3 | 45.1 | 12.7
| ASW | 46.4 | 39.3 | 14.3
| CHB | 71.1 | 28.9 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 77.1 | 21.9 | 1.0
| LWK | 39.6 | 50.0 | 10.4
| MEX | 68.4 | 31.6 | 0.0
| MKK | 57.1 | 36.4 | 6.5
| TSI | 0.0 | 0.0 | 0.0
| 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=7E-8
|OR=1.46
|ORtxt=[1.03-2.09]
|OA=1
}}

{{on chip | Affy GenomeWide 6}}