rs4086116, CYP2C9

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
WARFARIN SENSITIVITY (disorder)
CUI: C2608079
Disease: WARFARIN SENSITIVITY (disorder)
0.010 GeneticVariation BEFREE Carriers of the <i>CYP2C9</i> polymorphisms rs1057910 and rs4086116 had an increased risk of warfarin sensitivity compared to subjects with no or only one polymorphism. 31061616 2019