List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 3 by 3billion

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.7547C>T (p.Ala2516Val)	rs201073816	0.00009
NM_016239.4(MYO15A):c.581G>A (p.Arg194His)	rs1423809264	0.00001
NM_016239.4(MYO15A):c.10475dup (p.Leu3493fs)	rs2142436821
NM_016239.4(MYO15A):c.3928T>G (p.Cys1310Gly)	rs2142282291
NM_016239.4(MYO15A):c.4228C>T (p.His1410Tyr)	rs2142304025
NM_016239.4(MYO15A):c.8549G>C (p.Arg2850Pro)	rs568612566
NM_016239.4(MYO15A):c.9517G>A (p.Gly3173Arg)	rs2046776291

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