ClinVar Miner

List of variants reported as likely pathogenic for Autosomal recessive nonsyndromic hearing loss 16 by Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_153700.2(STRC):c.4027C>T (p.Gln1343Ter)	rs144948296	0.00009
NM_153700.2(STRC):c.4543C>T (p.Gln1515Ter)	rs756606635	0.00001

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