{{Rsnum
|rsid=378363
|Gene=PTPRD
|Chromosome=9
|position=9020223
|Orientation=plus
|GMAF=0.1892
|Gene_s=PTPRD
|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 | 56.6 | 39.8 | 3.5
| HCB | 74.8 | 23.7 | 1.5
| JPT | 74.8 | 22.5 | 2.7
| YRI | 49.0 | 40.0 | 11.0
| ASW | 70.2 | 28.1 | 1.8
| CHB | 74.8 | 23.7 | 1.5
| CHD | 77.6 | 17.8 | 4.7
| GIH | 65.0 | 27.0 | 8.0
| LWK | 54.1 | 40.4 | 5.5
| MEX | 59.6 | 36.8 | 3.5
| MKK | 53.9 | 38.3 | 7.8
| TSI | 74.3 | 21.8 | 4.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23793025
  |Trait=Migraine - clinic-based
  |Title=Genome-wide meta-analysis identifies new susceptibility loci for migraine.
  |RiskAllele=
  |Pval=8E-6
  |OR=1.14
  |ORtxt=[1.08-1.2]
  }}

{{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}}