ClinVar Miner

List of variants reported as uncertain significance for Autosomal dominant nonsyndromic hearing loss 22 by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004999.4(MYO6):c.178G>C (p.Glu60Gln)	rs757420692	0.00001
NM_139343.3(BIN1):c.1264-11_1270del	rs776737413

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