List of variants reported as likely pathogenic for autosomal recessive nonsyndromic hearing loss 32

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_003672.4(CDC14A):c.50-1G>T	rs2100872719
NM_003672.4(CDC14A):c.934C>G (p.Arg312Gly)	rs148737918
NM_003672.4(CDC14A):c.935G>A (p.Arg312Gln)	rs369245990
NM_003672.4(CDC14A):c.959A>C (p.Gln320Pro)	rs1339709390

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