List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 98

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_144991.3(TSPEAR):c.1915G>A (p.Asp639Asn)	rs138480801	0.00244
NM_144991.3(TSPEAR):c.364C>T (p.Arg122Trp)	rs146257403	0.00067
NM_144991.3(TSPEAR):c.1856+19C>T	rs182590005	0.00020
NM_144991.3(TSPEAR):c.533C>T (p.Pro178Leu)	rs782685093	0.00010
NM_144991.3(TSPEAR):c.304-5450G>T	rs143105755

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