{{Rsnum
|rsid=4979906
|Chromosome=10
|position=79444753
|Orientation=plus
|GMAF=0.3494
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 69.9 | 24.8 | 5.3
| HCB | 19.0 | 52.6 | 28.5
| JPT | 23.0 | 41.6 | 35.4
| YRI | 32.7 | 43.5 | 23.8
| ASW | 28.1 | 52.6 | 19.3
| CHB | 19.0 | 52.6 | 28.5
| CHD | 22.9 | 47.7 | 29.4
| GIH | 43.6 | 44.6 | 11.9
| LWK | 28.2 | 48.2 | 23.6
| MEX | 51.7 | 43.1 | 5.2
| MKK | 41.7 | 45.5 | 12.8
| TSI | 69.6 | 25.5 | 4.9
| 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=G
|Pval=0.000007
|OR=1.23
|ORtxt=[0.98-1.55]
|OA=1
}}

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