rs1045642, ABCB1

N. diseases: 214
Disease: Myopathy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Myopathy
CUI: C0026848
Disease: Myopathy
0.010 GeneticVariation BEFREE The evidence from the meta-analysis demonstrated that the ABCB1 C3435T polymorphism may represent a pharmacogenomic biomarker for predicting treatment outcomes in patients on statins and that statin treatment for more than 5 months can increase the risk of myopathy. 26438079 2015