List of variants reported as likely pathogenic for Autosomal recessive nonsyndromic hearing loss 3 by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.9620G>A (p.Arg3207His)	rs199621031	0.00026
NM_016239.4(MYO15A):c.6863C>T (p.Ser2288Leu)	rs886052676	0.00004
NM_016239.4(MYO15A):c.2629G>T (p.Glu877Ter)	rs771720649	0.00003
NM_016239.4(MYO15A):c.6787G>A (p.Gly2263Ser)	rs375459945	0.00001
NM_016239.4(MYO15A):c.3742C>T (p.Arg1248Trp)
NM_016239.4(MYO15A):c.8158G>A (p.Asp2720Asn)

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