Gene: SERPINC1 ×
Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909568
rs121909568
SERPINC1 ; ZBTB37
0.700 GeneticVariation UNIPROT The molecular basis of antithrombin deficiency in Belgian and Dutch families. 9759613

1998
dbSNP: rs1423630663
rs1423630663
SERPINC1
0.700 GeneticVariation UNIPROT The molecular basis of antithrombin deficiency in Belgian and Dutch families. 9759613

1998
dbSNP: rs1425532034
rs1425532034
SERPINC1
0.700 GeneticVariation UNIPROT The molecular basis of antithrombin deficiency in Belgian and Dutch families. 9759613

1998
dbSNP: rs483352854
rs483352854
SERPINC1
0.700 GeneticVariation UNIPROT The molecular basis of antithrombin deficiency in Belgian and Dutch families. 9759613

1998
dbSNP: rs1170430756
rs1170430756
SERPINC1
0.700 GeneticVariation UNIPROT Antithrombin mutation database: 2nd (1997) update. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. 9031473

1997
dbSNP: rs1170430756
rs1170430756
SERPINC1
0.700 GeneticVariation UNIPROT Antithrombin Morioka (Cys 95-Arg): a novel missense mutation causing type I antithrombin deficiency. 9157604

1997
dbSNP: rs121909568
rs121909568
SERPINC1 ; ZBTB37
0.700 GeneticVariation UNIPROT Antithrombin mutation database: 2nd (1997) update. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. 9031473

1997
dbSNP: rs121909568
rs121909568
SERPINC1 ; ZBTB37
0.700 GeneticVariation UNIPROT Antithrombin Morioka (Cys 95-Arg): a novel missense mutation causing type I antithrombin deficiency. 9157604

1997
dbSNP: rs1423630663
rs1423630663
SERPINC1
0.700 GeneticVariation UNIPROT Antithrombin Morioka (Cys 95-Arg): a novel missense mutation causing type I antithrombin deficiency. 9157604

1997
dbSNP: rs1423630663
rs1423630663
SERPINC1
0.700 GeneticVariation UNIPROT Antithrombin mutation database: 2nd (1997) update. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. 9031473

1997
dbSNP: rs1425532034
rs1425532034
SERPINC1
0.700 GeneticVariation UNIPROT Antithrombin mutation database: 2nd (1997) update. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. 9031473

1997
dbSNP: rs1425532034
rs1425532034
SERPINC1
0.700 GeneticVariation UNIPROT Antithrombin Morioka (Cys 95-Arg): a novel missense mutation causing type I antithrombin deficiency. 9157604

1997
dbSNP: rs483352854
rs483352854
SERPINC1
0.700 GeneticVariation UNIPROT Antithrombin Morioka (Cys 95-Arg): a novel missense mutation causing type I antithrombin deficiency. 9157604

1997
dbSNP: rs483352854
rs483352854
SERPINC1
0.700 GeneticVariation UNIPROT Antithrombin mutation database: 2nd (1997) update. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. 9031473

1997
dbSNP: rs1170430756
rs1170430756
SERPINC1
0.700 GeneticVariation UNIPROT Hereditary antithrombin deficiency: heterogeneity of the molecular basis and mortality in Dutch families. 7994035

1994
dbSNP: rs1170430756
rs1170430756
SERPINC1
0.700 GeneticVariation UNIPROT Antithrombin-Gly 424 Arg: a novel point mutation responsible for type 1 antithrombin deficiency and neonatal thrombosis. 8274732

1994
dbSNP: rs1170430756
rs1170430756
SERPINC1
0.700 GeneticVariation UNIPROT Three novel missense mutations in the antithrombin III (AT3) gene causing recurrent venous thrombosis. 7959685

1994
dbSNP: rs1170430756
rs1170430756
SERPINC1
0.700 GeneticVariation UNIPROT Thromboembolic disease due to thermolabile conformational changes of antithrombin Rouen-VI (187 Asn-->Asp) 7989582

1994
dbSNP: rs121909568
rs121909568
SERPINC1 ; ZBTB37
0.700 GeneticVariation UNIPROT Antithrombin-Gly 424 Arg: a novel point mutation responsible for type 1 antithrombin deficiency and neonatal thrombosis. 8274732

1994
dbSNP: rs121909568
rs121909568
SERPINC1 ; ZBTB37
0.700 GeneticVariation UNIPROT Three novel missense mutations in the antithrombin III (AT3) gene causing recurrent venous thrombosis. 7959685

1994
dbSNP: rs121909568
rs121909568
SERPINC1 ; ZBTB37
0.700 GeneticVariation UNIPROT Hereditary antithrombin deficiency: heterogeneity of the molecular basis and mortality in Dutch families. 7994035

1994
dbSNP: rs121909568
rs121909568
SERPINC1 ; ZBTB37
0.700 GeneticVariation UNIPROT Thromboembolic disease due to thermolabile conformational changes of antithrombin Rouen-VI (187 Asn-->Asp) 7989582

1994
dbSNP: rs1423630663
rs1423630663
SERPINC1
0.700 GeneticVariation UNIPROT Antithrombin-Gly 424 Arg: a novel point mutation responsible for type 1 antithrombin deficiency and neonatal thrombosis. 8274732

1994
dbSNP: rs1423630663
rs1423630663
SERPINC1
0.700 GeneticVariation UNIPROT Three novel missense mutations in the antithrombin III (AT3) gene causing recurrent venous thrombosis. 7959685

1994
dbSNP: rs1423630663
rs1423630663
SERPINC1
0.700 GeneticVariation UNIPROT Hereditary antithrombin deficiency: heterogeneity of the molecular basis and mortality in Dutch families. 7994035

1994