List of variants reported as likely pathogenic for autosomal dominant nonsyndromic hearing loss by Genome-Nilou Lab

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004700.4(KCNQ4):c.961G>A (p.Gly321Ser)	rs28939710	0.00001
NM_004700.4(KCNQ4):c.1438C>T (p.Gln480Ter)	rs1648636515

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