{{Rsnum
|rsid=909848
|Gene=PTGER3
|Chromosome=1
|position=70977467
|Orientation=plus
|GMAF=0.4096
|Gene_s=PTGER3
|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 | 40.7 | 42.5 | 16.8
| HCB | 24.1 | 52.6 | 23.4
| JPT | 31.0 | 52.2 | 16.8
| YRI | 40.8 | 44.2 | 15.0
| ASW | 36.8 | 49.1 | 14.0
| CHB | 24.1 | 52.6 | 23.4
| CHD | 21.1 | 57.8 | 21.1
| GIH | 37.6 | 49.5 | 12.9
| LWK | 42.7 | 50.9 | 6.4
| MEX | 27.6 | 34.5 | 37.9
| MKK | 44.2 | 44.9 | 10.9
| TSI | 44.1 | 46.1 | 9.8
| 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=7E-6
  |OR=.14
  |ORtxt=[0.081-0.206] unit increase
  |OA=1
}}

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