List of variants reported as likely pathogenic for autosomal dominant nonsyndromic hearing loss by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001145809.2(MYH14):c.2971G>A (p.Glu991Lys)	rs367588704	0.00001
NM_004086.3(COCH):c.292C>T (p.Arg98Ter)	rs756790858	0.00001
NM_002700.3(POU4F3):c.488del (p.His163fs)

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