ClinVar Miner

List of variants reported as likely pathogenic for Nonsyndromic hearing loss and deafness

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Total variants: 4
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HGVS dbSNP
NM_004004.6(GJB2):c.34G>T (p.Gly12Cys) rs104894408
NM_004700.4(KCNQ4):c.825G>C (p.Trp275Cys) rs956666801
NM_004999.4(MYO6):c.238C>T (p.Arg80Ter) rs727504567
NM_194248.3(OTOF):c.5332G>T (p.Val1778Phe) rs111033330

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