rs2032582, ABCB1

N. diseases: 97
Disease: CYP2D6 polymorphism ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
CYP2D6 polymorphism
CUI: C3203671
Disease: CYP2D6 polymorphism
0.010 GeneticVariation BEFREE Non-significant trend was noted for better treatment outcome of patients carrying at least one variant allele in the SNP rs2032582, while for the CYP2D6 polymorphism poor metabolizer phenotype resulted in worse outcome in comparison to extensive metabolizers subjects with HR of 4.04 (95 % CI 0.31-52.19). 26681084 2015