Analysis of the data for variants in genes associated with non-syndromic hearing loss (Supplemental Table S3), identified a novel single nucleotide variant in MYO6 (NM_004999.4, c.3526A > C/p.Ile1176Leu, I1176L) (Fig. 1b, right panel), a gene that has previously been associated with AD hearing loss [10]. The gene discussed is MYO6; the disease is hearing loss disorder.