ClinVar Miner

List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 30 by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_017433.5(MYO3A):c.3538G>A (p.Glu1180Lys)	rs184043065	0.00078
NM_017433.5(MYO3A):c.426T>G (p.His142Gln)	rs189595832	0.00029
NM_017433.5(MYO3A):c.3398+3A>G	rs373758358	0.00015

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