{{Rsnum
|rsid=563519
|Chromosome=11
|position=126158822
|Orientation=plus
|GMAF=0.4486
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 4.4 | 24.8 | 70.8
| HCB | 47.4 | 41.6 | 10.9
| JPT | 46.0 | 41.6 | 12.4
| YRI | 60.3 | 34.2 | 5.5
| ASW | 35.1 | 54.4 | 10.5
| CHB | 47.4 | 41.6 | 10.9
| CHD | 40.4 | 44.0 | 15.6
| GIH | 16.0 | 51.0 | 33.0
| LWK | 38.2 | 48.2 | 13.6
| MEX | 17.2 | 31.0 | 51.7
| MKK | 36.5 | 43.6 | 19.9
| TSI | 2.0 | 35.3 | 62.7
| 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=1.45
|ORtxt=[0.97-2.17]
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}