ClinVar Miner

List of variants studied for Autosomal dominant nonsyndromic hearing loss 11 by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_000260.4(MYO7A):c.2684G>A (p.Arg895His) rs1007895502 0.00003
NM_000260.4(MYO7A):c.1556G>A (p.Gly519Asp) rs111033206 0.00001
NM_000260.4(MYO7A):c.133-7C>T rs111033221
NM_000260.4(MYO7A):c.2003G>T (p.Arg668Leu) rs368575149

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