{{Rsnum
|rsid=548097
|Chromosome=13
|position=75202132
|Orientation=minus
|GMAF=0.06198
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 95.6 | 4.4 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 98.2 | 1.8 | 0.0
| YRI | 50.3 | 41.4 | 8.3
| ASW | 63.2 | 31.6 | 5.3
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 63.3 | 33.0 | 3.7
| MEX | 96.6 | 3.4 | 0.0
| MKK | 79.2 | 18.8 | 1.9
| TSI | 99.0 | 1.0 | 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=6E-7
|OR=1.62
|ORtxt=[1.00-2.63]
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}