List of variants reported as likely pathogenic for Autosomal dominant nonsyndromic hearing loss 11

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000260.4(MYO7A):c.652G>A (p.Asp218Asn)	rs201539845	0.00006
NM_000260.4(MYO7A):c.2371C>T (p.Arg791Cys)	rs782165016	0.00002
NM_000260.4(MYO7A):c.1556G>A (p.Gly519Asp)	rs111033206	0.00001
NM_000260.4(MYO7A):c.2558G>A (p.Arg853His)	rs111033437	0.00001
NM_000260.4(MYO7A):c.439C>T (p.Arg147Cys)	rs782808261	0.00001
NM_000260.4(MYO7A):c.6622C>T (p.Gln2208Ter)	rs747095250	0.00001
NM_000260.4(MYO7A):c.133del	rs1591224147
NM_000260.4(MYO7A):c.1531G>A (p.Asp511Asn)
NM_000260.4(MYO7A):c.2764AAG[1] (p.Lys923del)	rs1955175992
NM_000260.4(MYO7A):c.6409G>A (p.Gly2137Arg)	rs1223784415
NM_000260.4(MYO7A):c.689C>T (p.Ala230Val)	rs797044512

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