{{Rsnum
|rsid=4793501
|Chromosome=17
|position=70722593
|Orientation=plus
|GMAF=0.4284
|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 | 48.7 | 34.5
| HCB | 38.1 | 52.2 | 9.7
| JPT | 35.1 | 48.6 | 16.2
| YRI | 3.4 | 30.3 | 66.2
| ASW | 3.6 | 42.9 | 53.6
| CHB | 38.1 | 52.2 | 9.7
| CHD | 42.1 | 45.8 | 12.1
| GIH | 20.0 | 50.0 | 30.0
| LWK | 1.8 | 16.4 | 81.8
| MEX | 21.1 | 36.8 | 42.1
| MKK | 2.6 | 25.2 | 72.3
| TSI | 21.6 | 43.1 | 35.3
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23396134
  |Trait=Refractive error
  |Title=Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
  |RiskAllele=C
  |Pval=3E-8
  |OR=.08
  |ORtxt=[0.053-0.107] unit increase
  |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}}