List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 86

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001199107.2(TBC1D24):c.641G>A (p.Arg214His)	rs200324356	0.00068
NM_001199107.2(TBC1D24):c.643T>G (p.Trp215Gly)	rs761347854	0.00001
NM_001199107.2(TBC1D24):c.370C>A (p.Gln124Lys)	rs2141871461
NM_001199107.2(TBC1D24):c.523G>C (p.Ala175Pro)	rs2141871916
NM_001199107.2(TBC1D24):c.889C>T (p.Arg297Cys)	rs1351414664

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