{{Rsnum
|rsid=1656404
|Chromosome=2
|position=232515231
|Orientation=plus
|GMAF=0.1511
|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 | 67.7 | 27.7 | 4.6
| HCB | 95.6 | 4.4 | 0.0
| JPT | 97.8 | 2.2 | 0.0
| YRI | 61.3 | 33.9 | 4.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 95.6 | 4.4 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| 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=A
  |Pval=8E-11
  |OR=.15
  |ORtxt=[0.11-0.20] unit decrease
  |OA=1
}}

{{on chip | HumanOmni1Quad}}