ClinVar Miner

List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 79 by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001128228.3(TPRN):c.1725+5G>A	rs373827566	0.00004
NM_001128228.3(TPRN):c.1696C>T (p.Leu566Phe)	rs201404168	0.00001

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