{{Rsnum
|rsid=6445035
|Chromosome=3
|position=165762312
|Orientation=plus
|GMAF=0.1612
|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 | 3.1 | 30.8 | 66.2
| HCB | 2.2 | 35.6 | 62.2
| JPT | 6.7 | 26.7 | 66.7
| YRI | 0.0 | 34.9 | 65.1
| ASW | 0.0 | 0.0 | 0.0
| CHB | 2.2 | 35.6 | 62.2
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23508960
  |Trait=Aspirin hydrolysis (plasma)
  |Title=Aspirin hydrolysis in plasma is a variable function of butyrylcholinesterase and platelet-activating factor acetylhydrolase 1b2 (PAFAH1b2).
  |RiskAllele=A
  |Pval=9E-17
  |OR=NR
  |ORtxt=NR
  |OA=1
}}

{{on chip | FTDNA}}