Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Blood Coagulation Disorders
CUI: C0005779
Disease: Blood Coagulation Disorders
0.010 GeneticVariation BEFREE Hyperhomocyst(e)inemia and a common methylenetetrahydrofolate reductase mutation (Ala223Val MTHFR) in patients with inherited thrombophilic coagulation defects. 9409277 1997