{{Rsnum
|rsid=2721051
|Gene=LOC100289058
|Chromosome=13
|position=40536747
|Orientation=minus
|GMAF=0.07713
|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 | 17.7 | 82.3
| HCB | 0.0 | 0.7 | 99.3
| JPT | 0.0 | 0.0 | 100.0
| YRI | 1.4 | 14.4 | 84.2
| ASW | 0.0 | 14.0 | 86.0
| CHB | 0.0 | 0.7 | 99.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 8.9 | 91.1
| LWK | 0.0 | 14.7 | 85.3
| MEX | 1.7 | 10.3 | 87.9
| MKK | 0.6 | 23.9 | 75.5
| TSI | 1.0 | 25.5 | 73.5
| 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=G
|Pval=5E-10
|OR=0.24
|ORtxt=[0.16-0.32] unit decrease
|OA=1
}}

{{PMID Auto GWAS
  |PMID=23291589
  |Trait=Corneal structure
  |Title=Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.
  |RiskAllele=T
  |Pval=4E-14
  |OR=.17
  |ORtxt=[0.13-0.21] unit decrease
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}