List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 3 by Revvity Omics, Revvity

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.877G>A (p.Asp293Asn)	rs201415651	0.00051
NM_016239.4(MYO15A):c.5866C>T (p.Arg1956Trp)	rs185873402	0.00016
NM_016239.4(MYO15A):c.484C>T (p.Arg162Cys)	rs546203218	0.00015
NM_016239.4(MYO15A):c.4038+3A>G	rs564616200	0.00002
NM_016239.4(MYO15A):c.4351G>A (p.Asp1451Asn)	rs767270134	0.00001
NM_016239.4(MYO15A):c.6437G>A (p.Arg2146Gln)	rs760980785	0.00001
NM_016239.4(MYO15A):c.10006G>A (p.Glu3336Lys)
NM_016239.4(MYO15A):c.10508G>A (p.Arg3503His)
NM_016239.4(MYO15A):c.2766G>A (p.Val922=)
NM_016239.4(MYO15A):c.8771G>A (p.Arg2924His)

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