Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 462
Gene Symbol: SERPINC1
SERPINC1
0.340 GeneticVariation disease BEFREE SERPINC1 variants causing hereditary antithrombin deficiency in a Danish population. 30721820 2019
Entrez Id: 462
Gene Symbol: SERPINC1
SERPINC1
0.340 GeneticVariation disease BEFREE Impact of the type of SERPINC1 mutation and subtype of antithrombin deficiency on the thrombotic phenotype in hereditary antithrombin deficiency. 24196373 2014
Entrez Id: 462
Gene Symbol: SERPINC1
SERPINC1
0.340 Biomarker disease BEFREE An antithrombin III assay based on factor Xa inhibition provides a more reliable test to identify congenital antithrombin III deficiency than an assay based on thrombin inhibition. 8470046 1993
Entrez Id: 462
Gene Symbol: SERPINC1
SERPINC1
0.340 Biomarker disease BEFREE These results showed that in a neonate with congenital antithrombin III deficiency the antithrombin III concentrates would be administered to prevent neonatal arterial and venous thrombosis. 8327986 1993
Entrez Id: 462
Gene Symbol: SERPINC1
SERPINC1
0.340 Biomarker disease CTD_human [Treatment of deep venous thrombosis in the presence of a congenital antithrombin III deficiency. Apropos of the use of purified concentrates]. 6435583 1984
Entrez Id: 5627
Gene Symbol: PROS1
PROS1
0.010 GeneticVariation disease BEFREE This study suggests that congenital Antithrombin III deficiency constitutes a greater risk of thrombosis than congenital deficiencies of Protein C and Protein S. 8165635 1994
Entrez Id: 2159
Gene Symbol: F10
F10
0.010 Biomarker disease BEFREE An antithrombin III assay based on factor Xa inhibition provides a more reliable test to identify congenital antithrombin III deficiency than an assay based on thrombin inhibition. 8470046 1993