{{Rsnum
|rsid=4528684
|Chromosome=19
|position=14240762
|Orientation=plus
|GMAF=0.101
|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 | 79.6 | 17.7 | 2.7
| HCB | 90.4 | 8.8 | 0.7
| JPT | 71.7 | 26.5 | 1.8
| YRI | 66.7 | 31.3 | 2.0
| ASW | 52.6 | 40.4 | 7.0
| CHB | 90.4 | 8.8 | 0.7
| CHD | 94.5 | 5.5 | 0.0
| GIH | 88.1 | 11.9 | 0.0
| LWK | 69.7 | 27.5 | 2.8
| MEX | 94.7 | 5.3 | 0.0
| MKK | 58.1 | 38.1 | 3.9
| TSI | 90.2 | 9.8 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20400778
|Trait=Mortality among heart failure patients
|Title=Genomic Variation Associated with Mortality among Adults of European and African Ancestry with Heart Failure: The CHARGE Consortium
|RiskAllele=T
|Pval=0.000001
|OR=1.42
|ORtxt=[0.99-2.03]
|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}}