List of variants reported as likely benign for Autosomal recessive nonsyndromic hearing loss 3 by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.2680C>T (p.Pro894Ser)	rs76707172	0.00765
NM_016239.4(MYO15A):c.7655-7C>G	rs191171943	0.00211
NM_016239.4(MYO15A):c.10443G>A (p.Ala3481=)	rs190486507	0.00208
NM_016239.4(MYO15A):c.3203G>T (p.Cys1068Phe)	rs189061214	0.00047
NM_016239.4(MYO15A):c.7069G>A (p.Gly2357Ser)	rs201540919	0.00034

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