{{Rsnum
|rsid=3842788
|Gene=PTGS1
|Chromosome=9
|position=122377927
|Orientation=plus
|GMAF=0.09917
|Gene_s=PTGS1
|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 | 0.0 | 6.2 | 93.8
| HCB | 0.7 | 13.9 | 85.4
| JPT | 0.9 | 11.5 | 87.6
| YRI | 10.9 | 41.5 | 47.6
| ASW | 7.0 | 36.8 | 56.1
| CHB | 0.7 | 13.9 | 85.4
| CHD | 0.0 | 11.0 | 89.0
| GIH | 0.0 | 5.9 | 94.1
| LWK | 10.0 | 36.4 | 53.6
| MEX | 0.0 | 3.5 | 96.5
| MKK | 5.1 | 46.2 | 48.7
| TSI | 1.0 | 10.8 | 88.2
| HapMapRevision=28
}}{{PMID Auto
|PMID=21816595
|Title=A Promoter polymorphism (rs17222919, -1316T/G) of ALOX5AP is associated with intracerebral hemorrhage in Korean population
}}

{{PMID Auto
|PMID=17301694
|Title=Identification and functional characterization of polymorphisms in human cyclooxygenase-1 (PTGS1).
|OA=1
}}

{{PMID Auto
|PMID=18992148
|Title=Low-penetrance alleles predisposing to sporadic colorectal cancers: a French case-controlled genetic association study.
|OA=1
}}

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