{{Rsnum
|rsid=10519210
|Chromosome=15
|position=63445726
|Orientation=plus
|GMAF=0.06152
|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 | 0.0 | 5.4 | 94.6
| HCB | 0.0 | 0.7 | 99.3
| JPT | 0.0 | 0.0 | 100.0
| YRI | 4.8 | 34.0 | 61.2
| ASW | 3.5 | 29.8 | 66.7
| CHB | 0.0 | 0.7 | 99.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 4.0 | 96.0
| LWK | 4.5 | 32.7 | 62.7
| MEX | 0.0 | 10.3 | 89.7
| MKK | 0.6 | 16.7 | 82.7
| TSI | 0.0 | 2.9 | 97.1
| 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=1E-8
|OR=1.53
|ORtxt=[1.05-2.24]
|OA=1
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}