SPNS2 and auditory neuropathy: This table includes two carriers of clinically significant variants in genes associated with ANSD, as follows: the boy with CI carried both OTOF(NM_194248.3): c.2165G > C (p.Arg722Pro) and SPNS2(NM_001124758.3): c.310G > C (p.Ala104Pro) variants, while the girl with HA carried the CDH23(NM_022124.6): c.5386C > A (p.Pro1796Thr) variant.