{{Rsnum
|rsid=11071200
|Gene=PRTG
|Chromosome=15
|position=55657884
|Orientation=plus
|GMAF=0.1648
|Gene_s=PRTG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 5.3 | 31.9 | 62.8
| HCB | 0.0 | 2.2 | 97.8
| JPT | 0.0 | 4.4 | 95.6
| YRI | 8.2 | 46.3 | 45.6
| ASW | 7.0 | 45.6 | 47.4
| CHB | 0.0 | 2.2 | 97.8
| CHD | 0.0 | 7.3 | 92.7
| GIH | 2.0 | 11.9 | 86.1
| LWK | 9.2 | 47.7 | 43.1
| MEX | 0.0 | 20.7 | 79.3
| MKK | 9.1 | 42.9 | 48.1
| TSI | 4.0 | 33.7 | 62.4
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23648065
  |Trait=Adverse response to chemotherapy (neutropenia/leucopenia) (carboplatin)
  |Title=Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.
  |RiskAllele=T
  |Pval=9E-7
  |OR=8.24
  |ORtxt=[2.888-23.520]
  }}

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