{{Rsnum
|rsid=12447690
|Chromosome=16
|position=88264518
|Orientation=plus
|GMAF=0.4128
|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 | 16.8 | 34.5 | 48.7
| HCB | 4.4 | 31.4 | 64.2
| JPT | 8.0 | 38.4 | 53.6
| YRI | 66.7 | 29.9 | 3.4
| ASW | 50.9 | 40.4 | 8.8
| CHB | 4.4 | 31.4 | 64.2
| CHD | 7.3 | 32.1 | 60.6
| GIH | 16.8 | 57.4 | 25.7
| LWK | 67.3 | 30.0 | 2.7
| MEX | 10.3 | 50.0 | 39.7
| MKK | 51.3 | 39.1 | 9.6
| TSI | 17.6 | 47.1 | 35.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20485516
|Trait=Central corneal thickness
|Title=Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness
|RiskAllele=C
|Pval=9E-11
|OR=0.16
|ORtxt=[0.10-0.22] unit increase
|OA=1
}}

{{PMID Auto GWAS
|PMID=20719862
|Trait=None
|Title=New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8
|RiskAllele=G
|Pval=6E-22
|OR=0.16
|ORtxt=[0.13-0.19] unit decrease
}}
{{PMID Auto
|PMID=21098505
|Title=Collagen related genes influence glaucoma risk factor, central corneal thickness
}}

{{PMID Auto
|PMID=22661486
|Title=Genome-wide Analysis of Central Corneal Thickness in Primary Open-angle Glaucoma Cases in the NEIGHBOR and GLAUGEN consortia
|OA=1
}}

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