{{Rsnum
|rsid=11880198
|Gene=GNA15
|Chromosome=19
|position=3159771
|Orientation=plus
|GMAF=0.1433
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=GNA15
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 76.1 | 20.4 | 3.5
| HCB | 99.3 | 0.7 | 0.0
| JPT | 97.3 | 2.7 | 0.0
| YRI | 60.7 | 33.8 | 5.5
| ASW | 57.9 | 36.8 | 5.3
| CHB | 99.3 | 0.7 | 0.0
| CHD | 96.3 | 3.7 | 0.0
| GIH | 75.2 | 23.8 | 1.0
| LWK | 51.8 | 44.5 | 3.6
| MEX | 81.0 | 19.0 | 0.0
| MKK | 66.0 | 29.5 | 4.5
| TSI | 69.6 | 23.5 | 6.9
| 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=0.000006
|OR=1.23
|ORtxt=[0.98-1.54]
|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}}