Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Arterial Occlusive Diseases
CUI: C0003838
Disease: Arterial Occlusive Diseases
0.010 GeneticVariation BEFREE Factor V Leiden (a point mutation [1691G-->A] in the factor V gene), the prothrombin 20210G-->A mutation, and homozygosity for a common polymorphism in the methylene tetrahydrofolate reductase (MTHFR) gene (677C-->T) have been associated with arterial and venous thrombosis and arterial occlusive disease. 10360908 1999