{{Rsnum
|rsid=7044529
|Gene=COL5A1
|Chromosome=9
|position=134676205
|Orientation=plus
|GMAF=0.1887
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=COL5A1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 72.6 | 25.7 | 1.8
| HCB | 84.6 | 14.7 | 0.7
| JPT | 91.2 | 8.8 | 0.0
| YRI | 36.3 | 51.4 | 12.3
| ASW | 54.4 | 40.4 | 5.3
| CHB | 84.6 | 14.7 | 0.7
| CHD | 77.1 | 22.0 | 0.9
| GIH | 67.3 | 28.7 | 4.0
| LWK | 47.3 | 41.8 | 10.9
| MEX | 75.9 | 24.1 | 0.0
| MKK | 49.4 | 44.2 | 6.4
| TSI | 77.5 | 22.5 | 0.0
| 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=5E-8
|OR=0.13
|ORtxt=[0.09-0.18] unit decrease
}}

{{PMID Auto
|PMID=21098505
|Title=Collagen related genes influence glaucoma risk factor, central corneal thickness
}}

{{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
}}

{{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=5E-12
  |OR=.13
  |ORtxt=[0.091-0.169] unit decrease
  |OA=1
}}

{{PMID Auto
|PMID=23513063
|Title=Genetic association of COL5A1 variants in keratoconus patients suggests a complex connection between corneal thinning and keratoconus.
|OA=1
}}

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