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

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.10350+6T>C	rs2142431211
NM_016239.4(MYO15A):c.4195A>T (p.Ile1399Phe)	rs2142300755
NM_016239.4(MYO15A):c.4461C>A (p.Asn1487Lys)	rs201076604
NM_016239.4(MYO15A):c.5095T>G (p.Phe1699Val)	rs2142328605
NM_016239.4(MYO15A):c.5683G>A (p.Glu1895Lys)	rs2142341062
NM_016239.4(MYO15A):c.8474T>C (p.Leu2825Pro)	rs2142384242
NM_016239.4(MYO15A):c.9482A>C (p.Gln3161Pro)	rs2142399231
NM_016239.4(MYO15A):c.9820T>C (p.Tyr3274His)	rs2142412720

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