ClinVar Miner

List of variants reported as uncertain significance for Hearing loss, autosomal recessive 57 by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001195263.2(PDZD7):c.287G>T (p.Arg96Met)	rs758884514
NM_001195263.2(PDZD7):c.680G>A (p.Arg227His)	rs200730376
NM_001195263.2(PDZD7):c.806T>G (p.Ile269Ser)

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