{{Rsnum
|rsid=6747096
|Gene=SERPINE2
|Chromosome=2
|position=223998125
|Orientation=minus
|GMAF=0.2459
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Status=Merged
|Merged=12457
|Gene_s=SERPINE2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 68.1 | 30.1 | 1.8
| HCB | 83.1 | 16.9 | 0.0
| JPT | 73.5 | 24.8 | 1.8
| YRI | 23.4 | 47.6 | 29.0
| ASW | 32.1 | 55.4 | 12.5
| CHB | 83.1 | 16.9 | 0.0
| CHD | 71.6 | 25.7 | 2.8
| GIH | 60.0 | 33.0 | 7.0
| LWK | 22.0 | 46.8 | 31.2
| MEX | 72.4 | 25.9 | 1.7
| MKK | 32.1 | 40.4 | 27.6
| TSI | 55.4 | 39.6 | 5.0
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19604412
|Title=Absence of association between SERPINE2 genetic polymorphisms and chronic obstructive pulmonary disease in Han Chinese: a case-control cohort study
|OA=1
}}

{{PMID Auto
|PMID=19626039
|Title=Lack of replication of celiac disease risk variants reported in a Spanish population using an independent Spanish sample
}}

{{PMID|16358219|OA=1
}} The SERPINE2 gene is associated with chronic obstructive pulmonary disease.

{{PMID|16773582|OA=1
}} The SERPINE2 gene and chronic obstructive pulmonary disease.

{{PMID|18241860}} Combined functional and positional gene information for the identification of susceptibility variants in celiac disease.

{{PMID|18471539|OA=1
}} No evidence in a large UK collection for celiac disease risk variants reported by a Spanish study.

{{PMID|19949669|OA=1
}} SERPINE2 polymorphisms and chronic obstructive pulmonary disease.

{{PMID|20233420|OA=1
}} Cluster analysis in severe emphysema subjects using phenotype and genotype data: an exploratory investigation.

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}