{{Rsnum
|rsid=8017423
|Chromosome=14
|position=90213566
|Orientation=plus
|GMAF=0.5
|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 | 33.6 | 51.3 | 15.0
| HCB | 22.6 | 47.4 | 29.9
| JPT | 17.7 | 57.5 | 24.8
| YRI | 10.9 | 43.5 | 45.6
| ASW | 10.7 | 42.9 | 46.4
| CHB | 22.6 | 47.4 | 29.9
| CHD | 20.2 | 53.2 | 26.6
| GIH | 37.6 | 52.5 | 9.9
| LWK | 13.6 | 40.9 | 45.5
| MEX | 29.3 | 53.4 | 17.2
| MKK | 29.5 | 49.4 | 21.2
| TSI | 43.1 | 41.2 | 15.7
| 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=0.000007
|OR=1.64
|ORtxt=[0.94-2.78]
|OA=1
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}