In prediagnostic MM cases, for example, the MSLN-SNP rs3764246A > G showed a 33.3-fold OR, and the MSLN-SNP rs3764247A > C showed a 22.7-fold OR for a false-positive marker for the corresponding double mutations GG and CC, respectively, when compared with the common genotype in this subgroup. This evidence concerns the gene MSLN and Miyoshi myopathy.