List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 9 by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_194248.3(OTOF):c.4435G>A (p.Gly1479Ser)	rs145588516	0.00040
NM_194248.3(OTOF):c.4023+1G>A	rs186810296	0.00031
NM_194323.3(OTOF):c.3514C>T (p.Arg1172Trp)	rs530821443	0.00001
NM_194248.3(OTOF):c.3305A>G (p.Lys1102Arg)
NM_194248.3(OTOF):c.3348A>G (p.Arg1116=)	rs572579351

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