{{Rsnum
|rsid=2475335
|Gene=PTPRD
|Chromosome=9
|position=10260263
|Orientation=plus
|GMAF=0.2805
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 2.7 | 24.8 | 72.6
| HCB | 4.4 | 35.8 | 59.9
| JPT | 5.3 | 31.9 | 62.8
| YRI | 23.1 | 57.8 | 19.0
| ASW | 12.3 | 43.9 | 43.9
| CHB | 4.4 | 35.8 | 59.9
| CHD | 4.6 | 30.3 | 65.1
| GIH | 5.0 | 33.7 | 61.4
| LWK | 33.6 | 49.1 | 17.3
| MEX | 12.1 | 41.4 | 46.6
| MKK | 37.8 | 46.2 | 16.0
| TSI | 4.9 | 33.3 | 61.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20522523
|Trait=Partial epilepsies
|Title=Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study
|RiskAllele=
|Pval=0.000009
|OR=None
|ORtxt=None
|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 | Illumina Human 1M}}