List of variants reported as likely pathogenic for autosomal dominant nonsyndromic hearing loss by Genomic Research Center, Shahid Beheshti University of Medical Sciences

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004086.3(COCH):c.1150C>T (p.Arg384Cys)	rs756541797	0.00006
NM_000260.4(MYO7A):c.439C>T (p.Arg147Cys)	rs782808261	0.00001

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