Gene: SERPINC1 ×
Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs542881762
rs542881762
SERPINC1
T 0.700 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019
dbSNP: rs1170430756
rs1170430756
SERPINC1
0.700 GeneticVariation UNIPROT Type II antithrombin deficiency caused by a founder mutation Pro73Leu in the Finnish population: clinical picture. 23910795

2013
dbSNP: rs121909562
rs121909562
SERPINC1
A 0.700 CausalMutation CLINVAR Type II antithrombin deficiency caused by a founder mutation Pro73Leu in the Finnish population: clinical picture. 23910795

2013
dbSNP: rs121909568
rs121909568
SERPINC1 ; ZBTB37
0.700 GeneticVariation UNIPROT Type II antithrombin deficiency caused by a founder mutation Pro73Leu in the Finnish population: clinical picture. 23910795

2013
dbSNP: rs1423630663
rs1423630663
SERPINC1
0.700 GeneticVariation UNIPROT Type II antithrombin deficiency caused by a founder mutation Pro73Leu in the Finnish population: clinical picture. 23910795

2013
dbSNP: rs1425532034
rs1425532034
SERPINC1
0.700 GeneticVariation UNIPROT Type II antithrombin deficiency caused by a founder mutation Pro73Leu in the Finnish population: clinical picture. 23910795

2013
dbSNP: rs483352854
rs483352854
SERPINC1
0.700 GeneticVariation UNIPROT Type II antithrombin deficiency caused by a founder mutation Pro73Leu in the Finnish population: clinical picture. 23910795

2013
dbSNP: rs1487411568
rs1487411568
SERPINC1 ; ZBTB37
0.700 GeneticVariation UNIPROT The management of depression during pregnancy: a report from the American Psychiatric Association and the American College of Obstetricians and Gynecologists. 20027064

2010
dbSNP: rs758087836
rs758087836
SERPINC1
0.700 GeneticVariation UNIPROT The management of depression during pregnancy: a report from the American Psychiatric Association and the American College of Obstetricians and Gynecologists. 20027064

2010
dbSNP: rs1170430756
rs1170430756
SERPINC1
0.700 GeneticVariation UNIPROT Retinal vein occlusion associated with antithrombin deficiency secondary to a novel G9840C missense mutation. 16908819

2006
dbSNP: rs121909568
rs121909568
SERPINC1 ; ZBTB37
0.700 GeneticVariation UNIPROT Retinal vein occlusion associated with antithrombin deficiency secondary to a novel G9840C missense mutation. 16908819

2006
dbSNP: rs1423630663
rs1423630663
SERPINC1
0.700 GeneticVariation UNIPROT Retinal vein occlusion associated with antithrombin deficiency secondary to a novel G9840C missense mutation. 16908819

2006
dbSNP: rs1425532034
rs1425532034
SERPINC1
0.700 GeneticVariation UNIPROT Retinal vein occlusion associated with antithrombin deficiency secondary to a novel G9840C missense mutation. 16908819

2006
dbSNP: rs483352854
rs483352854
SERPINC1
0.700 GeneticVariation UNIPROT Retinal vein occlusion associated with antithrombin deficiency secondary to a novel G9840C missense mutation. 16908819

2006
dbSNP: rs1170430756
rs1170430756
SERPINC1
0.700 GeneticVariation UNIPROT Molecular basis of inherited antithrombin deficiency in Portuguese families: identification of genetic alterations and screening for additional thrombotic risk factors. 15164384

2004
dbSNP: rs121909568
rs121909568
SERPINC1 ; ZBTB37
0.700 GeneticVariation UNIPROT Molecular basis of inherited antithrombin deficiency in Portuguese families: identification of genetic alterations and screening for additional thrombotic risk factors. 15164384

2004
dbSNP: rs1423630663
rs1423630663
SERPINC1
0.700 GeneticVariation UNIPROT Molecular basis of inherited antithrombin deficiency in Portuguese families: identification of genetic alterations and screening for additional thrombotic risk factors. 15164384

2004
dbSNP: rs1425532034
rs1425532034
SERPINC1
0.700 GeneticVariation UNIPROT Molecular basis of inherited antithrombin deficiency in Portuguese families: identification of genetic alterations and screening for additional thrombotic risk factors. 15164384

2004
dbSNP: rs483352854
rs483352854
SERPINC1
0.700 GeneticVariation UNIPROT Molecular basis of inherited antithrombin deficiency in Portuguese families: identification of genetic alterations and screening for additional thrombotic risk factors. 15164384

2004
dbSNP: rs1170430756
rs1170430756
SERPINC1
0.700 GeneticVariation UNIPROT Intracerebral hemorrhage associated with a novel antithrombin gene mutation in a neonate. 11713457

2001
dbSNP: rs121909568
rs121909568
SERPINC1 ; ZBTB37
0.700 GeneticVariation UNIPROT Intracerebral hemorrhage associated with a novel antithrombin gene mutation in a neonate. 11713457

2001
dbSNP: rs1423630663
rs1423630663
SERPINC1
0.700 GeneticVariation UNIPROT Intracerebral hemorrhage associated with a novel antithrombin gene mutation in a neonate. 11713457

2001
dbSNP: rs1425532034
rs1425532034
SERPINC1
0.700 GeneticVariation UNIPROT Intracerebral hemorrhage associated with a novel antithrombin gene mutation in a neonate. 11713457

2001
dbSNP: rs483352854
rs483352854
SERPINC1
0.700 GeneticVariation UNIPROT Intracerebral hemorrhage associated with a novel antithrombin gene mutation in a neonate. 11713457

2001
dbSNP: rs1170430756
rs1170430756
SERPINC1
0.700 GeneticVariation UNIPROT The molecular basis of antithrombin deficiency in Belgian and Dutch families. 9759613

1998