rs4363657, SLCO1B1

N. diseases: 5
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 genomewide scan yielded a single strong association of myopathy with the rs4363657 single-nucleotide polymorphism (SNP) located within SLCO1B1 on chromosome 12 (P=4x10(-9)). 18650507 2008