List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 3 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.5693G>A (p.Arg1898Gln)	rs756752580	0.00001
NM_016239.4(MYO15A):c.10575C>G (p.Ser3525Arg)	rs201070092
NM_016239.4(MYO15A):c.2336C>T (p.Ser779Leu)
NM_016239.4(MYO15A):c.4072G>A (p.Gly1358Ser)
NM_016239.4(MYO15A):c.6830T>G (p.Leu2277Arg)

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