List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 79

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001128228.3(TPRN):c.2023G>A (p.Ala675Thr)	rs139520402	0.00070
NM_001128228.3(TPRN):c.770C>T (p.Pro257Leu)	rs745997859	0.00009
NM_001128228.3(TPRN):c.1725+5G>A	rs373827566	0.00004
NM_001128228.3(TPRN):c.691C>T (p.Arg231Trp)	rs886044045	0.00004
NM_001128228.3(TPRN):c.1936G>A (p.Glu646Lys)	rs370001536	0.00003
NM_001128228.3(TPRN):c.1696C>T (p.Leu566Phe)	rs201404168	0.00001
NM_001128228.3(TPRN):c.2057C>T (p.Pro686Leu)	rs727503520	0.00001

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