SERPINC1, serpin family C member 1, 462

N. diseases: 101; N. variants: 38
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.310 GeneticVariation phenotype BEFREE Inherited quantitative (type I) or qualitative (type II) antithrombin deficiency (ATD) due to mutations in the SERPINC1 gene is a well-known risk factor for venous thromboembolism. 28300866 2018
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.310 Biomarker phenotype CTD_human The effect of chlorotrianisene as postpartum lactation suppression on blood coagulation factors. 453287 1979