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

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001378609.3(OTOGL):c.236-2A>G	rs766564988	0.00009
NM_001378609.3(OTOGL):c.3213+1G>A	rs370730786	0.00004
NM_001378609.3(OTOGL):c.28A>G (p.Met10Val)	rs1277996676
NM_001378609.3(OTOGL):c.5211C>A (p.Cys1737Ter)	rs2137943672
NM_001378609.3(OTOGL):c.6162_6163del (p.Ala2055fs)

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