After applying the variant filtering criteria (Supplementary Information; Materials and Methods, Supplementary Fig. 3, and Supplementary Table 1), we identified eight different biallelic variants in MYH1 (myosin heavy chain 1; MIM: 16073) in five probands who were diagnosed with a recessive form of sensorineural hearing loss. The gene discussed is MYH1; the disease is sensorineural hearing loss disorder.