{{Rsnum
|rsid=2755237
|Chromosome=13
|position=40535292
|Orientation=plus
|GMAF=0.2328
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 72.6 | 27.4 | 0.0
| HCB | 40.9 | 51.8 | 7.3
| JPT | 47.8 | 43.4 | 8.8
| YRI | 56.5 | 36.7 | 6.8
| ASW | 63.2 | 35.1 | 1.8
| CHB | 40.9 | 51.8 | 7.3
| CHD | 44.0 | 45.0 | 11.0
| GIH | 82.2 | 17.8 | 0.0
| LWK | 53.6 | 40.9 | 5.5
| MEX | 81.0 | 17.2 | 1.7
| MKK | 51.9 | 43.6 | 4.5
| TSI | 60.8 | 35.3 | 3.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20719862
|Trait=None
|Title=New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8
|RiskAllele=A
|Pval=1E-8
|OR=0.17
|ORtxt=[0.11-0.23] unit increase
}}

{{PMID Auto
|PMID=20485516
|Title=Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness.
|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 | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}