rs201351580

This variant is located in the SERPINE1 gene.

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ClinVar annotation

Uncertain Significance★☆☆☆

2 submitters

Congenital plasminogen activator inhibitor type 1 deficiency; SERPINE1-related disorder

About SERPINE1

This gene encodes a member of the serine proteinase inhibitor (serpin) superfamily. This member is the principal inhibitor of tissue plasminogen activator (tPA) and urokinase (uPA), and hence is an inhibitor of fibrinolysis. The protein also functions as a component of innate antiviral immunity. Defects in this gene are the cause of plasminogen activator inhibitor-1 deficiency (PAI-1 deficiency), and high concentrations of the gene product are associated with thrombophilia. [provided by RefSeq, Aug 2020]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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