List of variants reported as likely benign for autosomal dominant nonsyndromic hearing loss 2A by Genome-Nilou Lab

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_004700.4(KCNQ4):c.1188C>T (p.Pro396=)	rs189541861	0.00222
NM_004700.4(KCNQ4):c.1231C>T (p.Arg411Cys)	rs199809248	0.00153
NM_004700.4(KCNQ4):c.465A>C (p.Gly155=)	rs145129529	0.00082
NM_004700.4(KCNQ4):c.1413T>C (p.Gly471=)	rs144810195	0.00041
NM_004700.4(KCNQ4):c.438G>A (p.Glu146=)	rs144434662	0.00025
NM_004700.4(KCNQ4):c.1572C>T (p.Asp524=)	rs568177070	0.00023
NM_004700.4(KCNQ4):c.735G>A (p.Gly245=)	rs147751558	0.00016
NM_004700.4(KCNQ4):c.1668C>T (p.Tyr556=)	rs140945833	0.00010
NM_004700.4(KCNQ4):c.176C>T (p.Pro59Leu)	rs775420649	0.00009
NM_004700.4(KCNQ4):c.2028C>T (p.Asp676=)	rs552843990	0.00009

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