{{Rsnum
|rsid=17114036
|Gene=PPAP2B
|Chromosome=1
|position=56497149
|Orientation=plus
|GMAF=0.08953
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PPAP2B
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 80.6 | 19.4 | 0.0
| HCB | 95.6 | 4.4 | 0.0
| JPT | 97.7 | 2.3 | 0.0
| YRI | 75.4 | 21.3 | 3.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 95.6 | 4.4 | 0.0
| 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=24262325
  |Trait=Coronary artery disease
  |Title=Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
  |RiskAllele=G
  |Pval=1E-8
  |OR=1.15
  |ORtxt=[1.1-1.22]
}}{{PMID Auto GWAS
|PMID=21378990
|Trait=Coronary heart disease
|Title=Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
|RiskAllele=A
|Pval=4E-19
|OR=1.1700
|ORtxt=[1.13-1.22]
|OA=1
}}
{{PMID Auto
|PMID=23202125
|Title=Large-scale association analysis identifies new risk loci for coronary artery disease.
}}
{{PMID Auto
|PMID=23161703
|Title=Influence of 23 coronary artery disease variants on recurrent myocardial infarction or cardiac death: the GRACE Genetics Study.
  }}
{{on chip | HumanOmni1Quad}}