ClinVar Miner

List of variants reported as uncertain significance for Autosomal dominant nonsyndromic hearing loss 20 by Laboratory of Prof. Karen Avraham, Tel Aviv University

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001614.5(ACTG1):c.166G>A (p.Asp56Asn)
NM_001614.5(ACTG1):c.46A>C (p.Met16Leu)
NM_001614.5(ACTG1):c.56C>T (p.Ala19Val)
NM_001614.5(ACTG1):c.692C>T (p.Ala231Val)

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