rs757240974, F2

N. diseases: 4
Disease: Factor II deficiency ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Factor II deficiency
CUI: C3203356
Disease: Factor II deficiency
0.010 GeneticVariation BEFREE Genetic analysis and functional characterization of prothrombins Corpus Christi (Arg382-Cys), Dhahran (Arg271-His), and hypoprothrombinemia. 8839854 1996