{{Rsnum
|rsid=7837791
|Chromosome=8
|position=59266527
|Orientation=plus
|GMAF=0.4568
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 31.9 | 47.8 | 20.4
| HCB | 25.5 | 49.6 | 24.8
| JPT | 28.3 | 38.1 | 33.6
| YRI | 12.9 | 48.3 | 38.8
| ASW | 15.8 | 42.1 | 42.1
| CHB | 25.5 | 49.6 | 24.8
| CHD | 21.1 | 56.0 | 22.9
| GIH | 63.4 | 31.7 | 5.0
| LWK | 13.6 | 39.1 | 47.3
| MEX | 5.2 | 37.9 | 56.9
| MKK | 17.9 | 55.8 | 26.3
| TSI | 22.5 | 55.9 | 21.6
| 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=T
  |Pval=4E-12
  |OR=.11
  |ORtxt=[0.077-0.135] 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}}