NQO1, NAD(P)H quinone dehydrogenase 1, 1728

N. diseases: 368; N. variants: 8
Disease: WARFARIN SENSITIVITY (disorder) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2608079
Disease: WARFARIN SENSITIVITY (disorder)
WARFARIN SENSITIVITY (disorder) 		0.300 Biomarker phenotype CTD_human Gene polymorphisms and the risk of warfarin-induced bleeding complications at therapeutic international normalized ratio (INR). 27581200 2016