List of variants reported as pathogenic for Autosomal recessive nonsyndromic hearing loss 3 by Illumina Laboratory Services, Illumina

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.9861C>T (p.Gly3287=)	rs372466080	0.00011
NM_016239.4(MYO15A):c.4198G>A (p.Val1400Met)	rs749136456	0.00006
NM_016239.4(MYO15A):c.6863C>T (p.Ser2288Leu)	rs886052676	0.00004

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