{{Rsnum
|rsid=672561
|Gene=PTGFR
|Chromosome=1
|position=78521617
|Orientation=plus
|GMAF=0.1781
|Gene_s=PTGFR
|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 | 9.7 | 28.3 | 61.9
| HCB | 0.0 | 15.3 | 84.7
| JPT | 0.0 | 7.1 | 92.9
| YRI | 10.2 | 46.3 | 43.5
| ASW | 5.3 | 33.3 | 61.4
| CHB | 0.0 | 15.3 | 84.7
| CHD | 0.9 | 10.1 | 89.0
| GIH | 3.0 | 33.7 | 63.4
| LWK | 8.2 | 40.9 | 50.9
| MEX | 1.7 | 22.4 | 75.9
| MKK | 6.4 | 40.4 | 53.2
| TSI | 3.9 | 26.5 | 69.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23382691
  |Trait=IgG glycosylation
  |Title=Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
  |RiskAllele=C
  |Pval=9E-6
  |OR=.17
  |ORtxt=[0.094-0.242] unit increase
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}