{{Rsnum
|rsid=729631
|Gene=SERPINE2
|Chromosome=2
|position=223980202
|Orientation=minus
|GMAF=0.3072
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=SERPINE2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 69.2 | 26.2 | 4.6
| HCB | 28.9 | 48.9 | 22.2
| JPT | 20.5 | 47.7 | 31.8
| YRI | 44.4 | 47.6 | 7.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 28.9 | 48.9 | 22.2
| 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
|PMID=19949669
|Title=SERPINE2 Polymorphisms and Chronic Obstructive Pulmonary Disease
|OA=1
}}

{{PMID Auto
|PMID=21611750
|Title=Association of SERPINE2 gene with the risk of chronic obstructive pulmonary disease and spirometric phenotypes in northern Han Chinese population
}}

{{PMID Auto
|PMID=22145704
|Title=SERPINE2 haplotype as a risk factor for panlobular type of emphysema
|OA=1
}}
{{PMID Auto
|PMID=16358219
|Title=The SERPINE2 gene is associated with chronic obstructive pulmonary disease.
|OA=1
}}

{{PMID Auto
|PMID=19017876
|Title=Genetic associations with hypoxemia and pulmonary arterial pressure in COPD.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}