No significant association was found between MM occurrence and PD1.3 G > A(rs11568821), PD1.6 G > A (rs10204525), PD1.10 C > G (rs5582977), PD-L1 + 8293 C > A (rs2890658), PD-L1 C > T (rs2297136) and PD-L1 G > C (rs4143815) SNVs in all genetic models (Fig. 1). This evidence concerns the gene PDCD1 and Miyoshi myopathy.