{{Rsnum
|rsid=9912468
|Gene=PRKCA
|Chromosome=17
|position=66322239
|Orientation=plus
|GMAF=0.4123
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=PRKCA
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 25.7 | 54.9 | 19.5
| HCB | 35.0 | 49.6 | 15.3
| JPT | 32.7 | 50.4 | 16.8
| YRI | 42.2 | 46.9 | 10.9
| ASW | 45.6 | 43.9 | 10.5
| CHB | 35.0 | 49.6 | 15.3
| CHD | 34.9 | 46.8 | 18.3
| GIH | 46.5 | 50.5 | 3.0
| LWK | 35.5 | 50.0 | 14.5
| MEX | 43.1 | 48.3 | 8.6
| MKK | 39.1 | 48.1 | 12.8
| TSI | 24.5 | 49.0 | 26.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21076409
|Trait=None
|Title=Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
|RiskAllele=G
|Pval=1E-8
|OR=0.3900
|ORtxt=[0.25-0.53] ms increase
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}