"Institute of Medical Genetics and Applied Genomics, University Hospit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1679197	NM_004999.4(MYO6):c.560del (p.Pro187fs)	MYO6 (P187fs)	Deletion (frameshift variant +2 more)	Autosomal dominant nonsyndromic hearing loss	GPathogenic
Select item 523937	NM_004999.4(MYO6):c.2751dup (p.Gln918fs)	MYO6 (Q918fs +1 more)	Duplication (frameshift variant +1 more)	Nonsyndromic genetic hearing loss	GLikely pathogenic FDA Recognized database