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

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000260.4(MYO7A):c.905G>A (p.Arg302His)	rs41298135	0.00281
NM_000260.4(MYO7A):c.4805G>A (p.Arg1602Gln)	rs139889944	0.00121
NM_000260.4(MYO7A):c.2283-20C>T	rs371838579	0.00068
NM_000260.4(MYO7A):c.4353C>T (p.Ala1451=)	rs372336857	0.00010
NM_000260.4(MYO7A):c.5355G>A (p.Pro1785=)	rs372311564	0.00008

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