List of variants reported as likely pathogenic for Autosomal dominant nonsyndromic hearing loss 13

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_080680.3(COL11A2):c.1218dup (p.Ala407fs)
NM_080680.3(COL11A2):c.1819-2A>G
NM_080680.3(COL11A2):c.2087_2090del (p.Glu696fs)	rs1583335192
NM_080680.3(COL11A2):c.3582+2_3582+3del
NM_080680.3(COL11A2):c.3852+1G>T	rs2150532832
NM_080680.3(COL11A2):c.4135C>T (p.Arg1379Ter)	rs121912950

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