{{Rsnum
|rsid=2659546
|Gene=PPP3CA
|Chromosome=4
|position=101116562
|Orientation=minus
|GMAF=0.1694
|Gene_s=PPP3CA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 15.6 | 84.4
| HCB | 4.4 | 33.3 | 62.2
| JPT | 6.4 | 39.4 | 54.1
| YRI | 17.5 | 44.8 | 37.8
| ASW | 5.6 | 48.1 | 46.3
| CHB | 4.4 | 33.3 | 62.2
| CHD | 0.0 | 0.0 | 0.0
| GIH | 2.0 | 14.1 | 83.8
| LWK | 12.3 | 45.3 | 42.5
| MEX | 3.5 | 29.8 | 66.7
| MKK | 5.8 | 47.4 | 46.8
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21979947
|Trait=None
|Title=A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries.
|RiskAllele=
|Pval=0.000004
|OR=1.6300
|ORtxt=[NR]
|OA=1
}}

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