ClinVar Miner

List of variants reported as uncertain significance for Nonsyndromic genetic hearing loss 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_000260.4(MYO7A):c.1358G>A (p.Cys453Tyr)	rs202080237	0.00011
NM_000260.4(MYO7A):c.2371C>T (p.Arg791Cys)	rs782165016	0.00002
NM_005422.4(TECTA):c.5431_5433del (p.Met1811del)

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