{{Rsnum
|rsid=2020918
|Chromosome=8
|position=42214920
|Orientation=minus
|GMAF=0.2824
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 38.4 | 44.6 | 17.0
| HCB | 47.4 | 46.0 | 6.6
| JPT | 49.6 | 42.5 | 8.0
| YRI | 73.5 | 23.8 | 2.7
| ASW | 71.9 | 28.1 | 0.0
| CHB | 47.4 | 46.0 | 6.6
| CHD | 51.4 | 41.3 | 7.3
| GIH | 63.4 | 33.7 | 3.0
| LWK | 70.9 | 24.5 | 4.5
| MEX | 72.4 | 24.1 | 3.4
| MKK | 61.5 | 34.6 | 3.8
| TSI | 44.1 | 42.2 | 13.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=22240314
|Title=Association of genetic variants of fibrinolytic system with stroke and stroke subtypes
}}

{{PMID Auto
|PMID=16356191
|Title=Regulatory polymorphisms in extracellular matrix protease genes and susceptibility to rheumatoid arthritis: a case-control study.
|OA=1
}}

{{PMID Auto
|PMID=19526059
|Title=Polymorphic variation of genes in the fibrinolytic system and the risk of ovarian cancer.
|OA=1
}}

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