ClinVar Miner

List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 3 by Genetic Testing Center for Deafness, Department of Otolaryngology Head & Neck Surgery, Institute of Otolaryngology, Chinese PLA General Hospital

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.7547C>T (p.Ala2516Val)	rs201073816	0.00009
NM_016239.4(MYO15A):c.7633G>T (p.Asp2545Tyr)	rs577721556	0.00001

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