List of variants reported as pathogenic for Autosomal recessive nonsyndromic hearing loss 3 by Division of Human Genetics, Children's Hospital of Philadelphia

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.8714-1G>A	rs377015931	0.00006
NM_016239.4(MYO15A):c.5925G>A (p.Trp1975Ter)	rs375290498	0.00005
NM_016239.4(MYO15A):c.3311dup (p.Gly1104_Glu1105insTer)	rs794729637
NM_016239.4(MYO15A):c.625G>T (p.Glu209Ter)	rs571594379

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