{{Rsnum
|rsid=4507975
|Gene=PAPPA2
|Chromosome=1
|position=176715296
|Orientation=plus
|GMAF=0.2805
|Gene_s=PAPPA2
|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 | 45.0 | 46.8 | 8.1
| HCB | 83.9 | 15.3 | 0.7
| JPT | 92.0 | 8.0 | 0.0
| YRI | 22.6 | 53.4 | 24.0
| ASW | 49.1 | 38.6 | 12.3
| CHB | 83.9 | 15.3 | 0.7
| CHD | 86.2 | 11.0 | 2.8
| GIH | 37.0 | 51.0 | 12.0
| LWK | 17.3 | 47.3 | 35.5
| MEX | 70.7 | 25.9 | 3.4
| MKK | 31.4 | 46.2 | 22.4
| TSI | 44.1 | 44.1 | 11.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23509962
  |Trait=Venous thromboembolism (gene x gene interaction)
  |Title=A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.
  |RiskAllele=
  |Pval=4E-9
  |OR=1.54
  |ORtxt=[NR]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}