{{Rsnum
|rsid=2305619
|Gene=PTX3
|Chromosome=3
|position=157437072
|Orientation=plus
|GMAF=0.4509
|Gene_s=PTX3,VEPH1
|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 | 25.7 | 48.7 | 25.7
| HCB | 11.7 | 50.4 | 38.0
| JPT | 7.1 | 50.4 | 42.5
| YRI | 32.7 | 53.1 | 14.3
| ASW | 33.3 | 59.6 | 7.0
| CHB | 11.7 | 50.4 | 38.0
| CHD | 15.6 | 42.2 | 42.2
| GIH | 15.8 | 40.6 | 43.6
| LWK | 31.8 | 45.5 | 22.7
| MEX | 12.1 | 53.4 | 34.5
| MKK | 22.4 | 51.3 | 26.3
| TSI | 28.4 | 48.0 | 23.5
| HapMapRevision=28
}}{{PMID Auto
|PMID=22822025
|Title=Variation in PTX3 is Associated With Primary Graft Dysfunction After          Lung Transplantation
|OA=1
}}

{{PMID Auto
|PMID=19503741
|Title=Coding variant Met72Thr in the PEDF gene and risk of neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.
|OA=1
}}

{{PMID Auto
|PMID=19753309
|Title=SOD2 gene polymorphisms in neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.
|OA=1
}}

{{PMID Auto
|PMID=20157514
|Title=Positive association of common variants in CD36 with neovascular age-related macular degeneration.
|OA=1
}}

{{PMID Auto
|PMID=23285251
|Title=Influence of pentraxin 3 (PTX3) genetic variants on myocardial infarction risk and PTX3 plasma levels
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}