Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Congenital Bleeding Disorder
CUI: C3641106
Disease: Congenital Bleeding Disorder
0.010 GeneticVariation BEFREE Impact of IFNL4 rs12979860 and rs8099917 polymorphisms on response to Peg-Interferon-α and Ribavirin in patients with congenital bleeding disorder and chronic hepatitis C. 27735085 2017