List of variants reported as likely pathogenic for Autosomal recessive nonsyndromic hearing loss 3 by Deafness Molecular Diagnostic Center, Chinese PLA General Hospital

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.3904del (p.Met1302fs)	rs2142282007
NM_016239.4(MYO15A):c.4482+2T>C	rs2142307505
NM_016239.4(MYO15A):c.4538C>T (p.Ala1513Val)	rs2142315607
NM_016239.4(MYO15A):c.5835T>G (p.Tyr1945Ter)	rs2142343642
NM_016239.4(MYO15A):c.6045A>T (p.Ala2015=)	rs2142347739
NM_016239.4(MYO15A):c.6551_6552del (p.Cys2184fs)	rs2142360575

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