List of variants reported as pathogenic for autosomal recessive nonsyndromic hearing loss 3 by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.2419C>T (p.Gln807Ter)	rs1233145763	0.00001
NM_016239.4(MYO15A):c.1137del (p.Tyr380fs)	rs769260536
NM_016239.4(MYO15A):c.1185dup (p.Glu396fs)	rs772536599
NM_016239.4(MYO15A):c.7124_7127del (p.Asp2375fs)	rs780170125

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