{{Rsnum
|rsid=9938149
|Chromosome=16
|position=88298034
|Orientation=plus
|GMAF=0.2567
|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 | 44.2 | 39.8 | 15.9
| HCB | 89.8 | 10.2 | 0.0
| JPT | 95.6 | 4.4 | 0.0
| YRI | 46.9 | 41.5 | 11.6
| ASW | 50.9 | 42.1 | 7.0
| CHB | 89.8 | 10.2 | 0.0
| CHD | 84.4 | 15.6 | 0.0
| GIH | 45.5 | 46.5 | 7.9
| LWK | 32.7 | 53.6 | 13.6
| MEX | 48.3 | 44.8 | 6.9
| MKK | 27.6 | 51.3 | 21.2
| TSI | 32.4 | 51.0 | 16.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=21098505
|Title=Collagen related genes influence glaucoma risk factor, central corneal thickness
}}

{{PMID Auto
|PMID=22814818
|Title=Population-based meta-analysis in Caucasians confirms association with COL5A1 and ZNF469 but not COL8A2 with central corneal thickness
}}

{{PMID|20485516|OA=1
}} Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness.

{{PMID Auto GWAS
  |PMID=23291589
  |Trait=Corneal structure
  |Title=Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.
  |RiskAllele=A
  |Pval=2E-49
  |OR=.17
  |ORtxt=[0.15-0.19] unit increase
  |OA=1
}}

{{PMID Auto
|PMID=24265017
|Title=Evaluating the association between keratoconus and the corneal thickness genes in an independent Australian Population
}}

{{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 | Illumina Human 1M}}