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

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.4198G>A (p.Val1400Met)	rs749136456	0.00006
NM_016239.4(MYO15A):c.10573del (p.Ser3525fs)	rs1270302810	0.00004
NM_016239.4(MYO15A):c.6371G>A (p.Arg2124Gln)	rs368053088	0.00004
NM_016239.4(MYO15A):c.9517+2T>C	rs1322423998	0.00004
NM_016239.4(MYO15A):c.9765_9766insGG (p.Ile3256fs)	rs757070287	0.00001
NM_016239.4(MYO15A):c.6864_6874del (p.Asp2289fs)	rs2142363190

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