{{Rsnum
|rsid=3796804
|Gene=PRKG2
|Chromosome=4
|position=81088553
|Orientation=plus
|GMAF=0.3384
|Gene_s=PRKG2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 87.6 | 12.4 | 0.0
| HCB | 34.8 | 54.1 | 11.1
| JPT | 39.8 | 44.2 | 15.9
| YRI | 7.5 | 32.0 | 60.5
| ASW | 10.5 | 47.4 | 42.1
| CHB | 34.8 | 54.1 | 11.1
| CHD | 37.0 | 46.3 | 16.7
| GIH | 44.6 | 44.6 | 10.9
| LWK | 2.8 | 29.4 | 67.9
| MEX | 69.0 | 24.1 | 6.9
| MKK | 11.6 | 49.0 | 39.4
| TSI | 80.4 | 18.6 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22174851
|Trait=None
|Title=Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure.
|RiskAllele=
|Pval=0.000009
|OR=0
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}