{{Rsnum
|rsid=7849581
|Gene=PTPRD
|Chromosome=9
|position=9924724
|Orientation=plus
|GMAF=0.241
|Gene_s=PTPRD
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 99.1 | 0.9 | 0.0
| HCB | 52.9 | 38.2 | 8.8
| JPT | 56.8 | 38.7 | 4.5
| YRI | 14.9 | 53.2 | 31.9
| ASW | 28.1 | 49.1 | 22.8
| CHB | 52.9 | 38.2 | 8.8
| CHD | 54.2 | 41.1 | 4.7
| GIH | 72.7 | 21.2 | 6.1
| LWK | 12.0 | 52.8 | 35.2
| MEX | 42.6 | 48.1 | 9.3
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23049088
  |Trait=Myopia (pathological)
  |Title=A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population.
  |RiskAllele=
  |Pval=9E-7
  |OR=NR
  |ORtxt=NR
  }}

{{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}}