List of variants reported as pathogenic for Autosomal recessive nonsyndromic hearing loss 3 by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.3385C>T (p.Arg1129Ter)	rs748868741	0.00002
NM_016239.4(MYO15A):c.5896C>T (p.Arg1966Ter)	rs765468034	0.00001
NM_016239.4(MYO15A):c.8968-1G>T	rs746051220	0.00001
NM_016239.4(MYO15A):c.996C>G (p.Tyr332Ter)	rs759523751	0.00001

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