{{Rsnum
|rsid=8111998
|Chromosome=19
|position=22558873
|Orientation=plus
|GMAF=0.2218
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 90.8 | 7.7 | 1.5
| HCB | 67.4 | 32.6 | 0.0
| JPT | 68.2 | 29.5 | 2.3
| YRI | 5.6 | 37.1 | 57.3
| ASW | 16.4 | 45.5 | 38.2
| CHB | 67.4 | 32.6 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 14.7 | 47.7 | 37.6
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| 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=8E-7
|OR=1.7100
|ORtxt=[NR]
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}