Variant: rs61865606

present in Gene: LOC105378568 present in Chromosome: 10 Position on Chromosome: 132440647 Alleles of this Variant: T/C;G

rs61865606 in LOC105378568 gene and Myopathy PMID 31220337 2019 Genomewide Association Study of Statin-Induced Myopathy in Patients Recruited Using the UK Clinical Practice Research Datalink.