ClinVar Miner

List of variants reported as likely pathogenic for Childhood onset hearing loss by National Institute on Deafness and Communication Disorders, National Institutes of Health

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_006383.4(CIB2):c.556C>T (p.Arg186Trp)	rs370359511	0.00024
NM_016239.4(MYO15A):c.7006C>T (p.Gln2336Ter)	rs1169954783	0.00001
NM_022124.6(CDH23):c.3176A>T (p.Asp1059Val)	rs1865887896

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