{{Rsnum
|rsid=987539
|Gene=PON2
|Chromosome=7
|position=95407680
|Orientation=plus
|GMAF=0.3485
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=PON2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 27.4 | 54.0 | 18.6
| HCB | 0.7 | 26.5 | 72.8
| JPT | 0.0 | 19.5 | 80.5
| YRI | 10.2 | 45.6 | 44.2
| ASW | 12.3 | 47.4 | 40.4
| CHB | 0.7 | 26.5 | 72.8
| CHD | 4.6 | 27.5 | 67.9
| GIH | 10.9 | 42.6 | 46.5
| LWK | 3.6 | 40.9 | 55.5
| MEX | 8.6 | 36.2 | 55.2
| MKK | 16.0 | 42.3 | 41.7
| TSI | 22.8 | 57.4 | 19.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=21223581
|Title=Association analysis of PON2 genetic variants with serum paraoxonase activity and systemic lupus erythematosus
|OA=1
}}

{{PMID Auto
|PMID=18618303
|Title=A common haplotype within the PON1 promoter region is associated with sporadic ALS.
|OA=1
}}

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