We confirmed the association between rs1060896 and MM risk (p = 0.0072) and found that 5/7 alleles (T for ALDH3A2 rs72547554, A for SLC29A1 rs8187630, T for SLC28A1 rs8187737, A for PPARD rs6937483, A for ADH1B rs1229984) are also present in our internal dataset, although at a very low frequency, but significantly associated with MM risk (Table 1). The gene discussed is PPARD; the disease is Miyoshi myopathy.