ClinVar Miner

List of variants reported as likely pathogenic for Deafness, autosomal dominant 10

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Total variants: 3
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HGVS dbSNP
NM_004100.4(EYA4):c.1109G>A (p.Arg370His) rs143936434
NM_004100.4(EYA4):c.1739-1G>A rs797045088
NM_004100.5(EYA4):c.1347C>G (p.Tyr449Ter)

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