List of variants reported as likely pathogenic for Autosomal dominant nonsyndromic hearing loss 11; Autosomal recessive nonsyndromic hearing loss 2; Usher syndrome type 1

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000260.4(MYO7A):c.5618G>A (p.Arg1873Gln)	rs397516322	0.00006
NM_000260.4(MYO7A):c.631A>G (p.Ser211Gly)	rs111033486	0.00005
NM_000260.4(MYO7A):c.1190C>A (p.Ala397Asp)	rs1555067667	0.00001
NM_000260.4(MYO7A):c.2187+1G>A	rs111033290	0.00001
NM_000260.4(MYO7A):c.2863G>A (p.Gly955Ser)	rs781988557	0.00001
NM_000260.4(MYO7A):c.5573T>C (p.Leu1858Pro)	rs368657015	0.00001
NM_000260.4(MYO7A):c.1183C>T (p.Arg395Cys)	rs782279338
NM_000260.4(MYO7A):c.285+2T>G	rs782292032
NM_000260.4(MYO7A):c.2914C>T (p.Arg972Ter)	rs782281371
NM_000260.4(MYO7A):c.397C>T (p.His133Tyr)	rs111033403
NM_000260.4(MYO7A):c.5143GAG[1] (p.Glu1716del)	rs1555102843
NM_000260.4(MYO7A):c.6479G>A (p.Trp2160Ter)

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