{{Rsnum
|rsid=1952138
|Gene=PRKG1
|Chromosome=10
|position=53262633
|Orientation=plus
|GMAF=0.1382
|Gene_s=PRKG1
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 65.5 | 29.2 | 5.3
| HCB | 88.3 | 11.7 | 0.0
| JPT | 93.8 | 6.2 | 0.0
| YRI | 92.5 | 7.5 | 0.0
| ASW | 82.5 | 14.0 | 3.5
| CHB | 88.3 | 11.7 | 0.0
| CHD | 93.6 | 6.4 | 0.0
| GIH | 88.1 | 11.9 | 0.0
| LWK | 80.0 | 20.0 | 0.0
| MEX | 82.8 | 13.8 | 3.4
| MKK | 68.6 | 28.2 | 3.2
| TSI | 57.8 | 36.3 | 5.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23382691
  |Trait=IgG glycosylation
  |Title=Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
  |RiskAllele=C
  |Pval=3E-6
  |OR=.17
  |ORtxt=[0.1-0.24] unit decrease
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}