ClinVar Miner

List of variants studied for Autosomal dominant nonsyndromic hearing loss 15 by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_002700.3(POU4F3):c.553C>T (p.Arg185Cys) rs746613906 0.00001
NM_002700.3(POU4F3):c.745C>A (p.Gln249Lys) rs1465371108

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