{{Rsnum
|rsid=12229663
|Gene=PTPRR
|Chromosome=12
|position=70856216
|Orientation=plus
|GMAF=0.2498
|Gene_s=PTPRR
|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 | 60.2 | 34.5 | 5.3
| HCB | 39.8 | 48.1 | 12.0
| JPT | 42.7 | 47.3 | 10.0
| YRI | 62.6 | 33.3 | 4.1
| ASW | 75.4 | 22.8 | 1.8
| CHB | 39.8 | 48.1 | 12.0
| CHD | 28.7 | 56.5 | 14.8
| GIH | 62.4 | 32.7 | 5.0
| LWK | 63.9 | 34.3 | 1.9
| MEX | 74.1 | 24.1 | 1.7
| MKK | 76.9 | 21.8 | 1.3
| TSI | 56.4 | 43.6 | 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=G
  |Pval=5E-9
  |OR=.10
  |ORtxt=[0.066-0.132] unit increase
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}