List of variants reported as pathogenic for autosomal dominant nonsyndromic hearing loss by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001614.5(ACTG1):c.791C>T (p.Pro264Leu)	rs104894546
NM_004999.4(MYO6):c.2839C>T (p.Arg947Ter)	rs876657653
NM_004999.4(MYO6):c.406C>T (p.Arg136Ter)

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