rs6025, F5

N. diseases: 43
Disease: Severe hereditary factor VIII deficiency disease ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Severe hereditary factor VIII deficiency disease
CUI: C0272322
Disease: Severe hereditary factor VIII deficiency disease
0.010 GeneticVariation BEFREE The present cohort study was performed to investigate the impact of the factor 5 rs6025 [F5] and the factor 2 rs1799963 [F2] mutations on high-titer inhibitor development [HRI] in patients with severe/moderate-severe hemophilia A [HA]. 24485400 2014