rs899127658, F2

N. diseases: 82
Disease: Protein S Deficiency ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Protein S Deficiency
CUI: C0242666
Disease: Protein S Deficiency
0.030 GeneticVariation BEFREE In conclusion, coagulant factor V gene G1691A mutation and protein S deficiency constitute important genetic risk factors in patients with VTE in Eastern Algeria. 26304686 2017
Protein S Deficiency
CUI: C0242666
Disease: Protein S Deficiency
0.030 GeneticVariation BEFREE Utility of thrombin-generation assay in the screening of factor V G1691A (Leiden) and prothrombin G20210A mutations and protein S deficiency. 16469858 2006
Protein S Deficiency
CUI: C0242666
Disease: Protein S Deficiency
0.030 GeneticVariation BEFREE Besides antithrombin, protein C, and protein S deficiencies, none of which was found in our patient group, factor V G1691A (FV G1691A), prothrombin G20210A (PT G20210A) mutations, and methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphisms were studied. 12506156 2003