rs1799963, F2

N. diseases: 25
Disease: Cerebrovascular accident ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
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
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
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
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
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
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
0.810 SusceptibilityMutation CLINVAR The genetics of venous thromboembolism. A meta-analysis involving approximately 120,000 cases and 180,000 controls. 19652888 2009
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
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
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
0.810 SusceptibilityMutation CLINVAR Increased efficiency of mRNA 3' end formation: a new genetic mechanism contributing to hereditary thrombophilia. 11443298 2001