{{Rsnum
|rsid=2273788
|Gene=PTGR1
|Chromosome=9
|position=111586337
|Orientation=plus
|GMAF=0.2429
|Gene_s=PTGR1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 52.2 | 43.4 | 4.4
| HCB | 66.4 | 26.3 | 7.3
| JPT | 81.4 | 17.7 | 0.9
| YRI | 46.2 | 40.6 | 13.3
| ASW | 35.1 | 54.4 | 10.5
| CHB | 66.4 | 26.3 | 7.3
| CHD | 62.0 | 36.1 | 1.9
| GIH | 48.5 | 40.6 | 10.9
| LWK | 30.6 | 51.9 | 17.6
| MEX | 59.6 | 35.1 | 5.3
| MKK | 35.7 | 51.9 | 12.3
| TSI | 68.3 | 29.7 | 2.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23314186
  |Trait=Monocyte count
  |Title=Genetic variation associated with circulating monocyte count in the eMERGE Network.
  |RiskAllele=A
  |Pval=5E-7
  |OR=.16
  |ORtxt=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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}