rs4653436, None

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 In our study population, no significant correlation could be detected between CYP2C9*3, CYP2C9C-65 (rs9332127), CYP4F2 rs2108622, GGCX rs12714145, EPHX1 rs4653436 and PROC rs1799809 with warfarin sensitivity. 21639946 2011