{{Rsnum
|rsid=10487132
|Gene=PON3
|Chromosome=7
|position=95390993
|Orientation=plus
|GMAF=0.1956
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PON3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 27.4 | 55.8 | 16.8
| HCB | 97.8 | 2.2 | 0.0
| JPT | 98.2 | 1.8 | 0.0
| YRI | 80.3 | 18.4 | 1.4
| ASW | 78.9 | 19.3 | 1.8
| CHB | 97.8 | 2.2 | 0.0
| CHD | 97.2 | 2.8 | 0.0
| GIH | 57.4 | 35.6 | 6.9
| LWK | 96.4 | 3.6 | 0.0
| MEX | 70.7 | 25.9 | 3.4
| MKK | 77.6 | 19.9 | 2.6
| TSI | 37.3 | 52.9 | 9.8
| HapMapRevision=28
}}

{{PMID|19321847|OA=1
}} No association between [[rs10487132]] and amyotrophic lateral sclerosis was seen in this large meta-analysis.

{{PMID Auto
|PMID=16822964
|Title=Paraoxonase cluster polymorphisms are associated with sporadic ALS.
}}

{{PMID Auto
|PMID=17702780
|Title=Paraoxonase promoter and intronic variants modify risk of sporadic amyotrophic lateral sclerosis.
|OA=1
}}

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

{{PMID Auto
|PMID=22884547
|Title=Association analysis of PON polymorphisms in sporadic ALS in a Chinese population.
}}

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