List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 84B by Revvity Omics, Revvity

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001378609.3(OTOGL):c.5350G>A (p.Val1784Met)	rs571909899	0.00015
NM_001378609.3(OTOGL):c.3434C>T (p.Ala1145Val)	rs374368341	0.00006
NM_001378609.3(OTOGL):c.1694A>G (p.Gln565Arg)
NM_001378609.3(OTOGL):c.6235T>C (p.Cys2079Arg)

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