Likewise, rs4149056 (c.521 T > C, p.Val174Ala) in SLCO1B1, which encodes for the hepatic transporter OATP1B1 for statin uptake, did not modify the long‐term trajectory of muscle function and mass, despite its established link with statin‐associated muscle symptoms and myopathy risk [30, 31]. This evidence concerns the gene SLCO1B1 and myopathy.