Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799963
rs1799963
F2
A 0.810 GeneticVariation GWASCAT Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis. 26908601

2016
dbSNP: rs1799963
rs1799963
F2
A 0.810 SusceptibilityMutation CLINVAR Prevalence and Geographical Variation of Prothrombin G20210A Mutation in Patients with Cerebral Vein Thrombosis: A Systematic Review and Meta-Analysis. 27031503

2016
dbSNP: rs1799963
rs1799963
F2
0.810 GeneticVariation BEFREE In multinomial multivariate adjusted analysis, rs1799963 was exclusively associated with undetermined stroke (OR: 3.67; 95% CI: 1.52-8.85; p = 0.004). 25897999

2015
dbSNP: rs1799963
rs1799963
F2
A 0.810 SusceptibilityMutation CLINVAR The genetics of venous thromboembolism. A meta-analysis involving approximately 120,000 cases and 180,000 controls. 19652888

2009
dbSNP: rs1799963
rs1799963
F2
A 0.810 SusceptibilityMutation CLINVAR The prothrombin 3'end formation signal reveals a unique architecture that is sensitive to thrombophilic gain-of-function mutations. 15059842

2004
dbSNP: rs1799963
rs1799963
F2
A 0.810 SusceptibilityMutation CLINVAR Increased efficiency of mRNA 3' end formation: a new genetic mechanism contributing to hereditary thrombophilia. 11443298

2001