List of variants reported as pathogenic for autosomal dominant nonsyndromic hearing loss by Laboratory of Molecular Genetics, Brain Korea 21 PLUS Project for Medical Sciences, Yonsei University College of Medicine

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_004700.4(KCNQ4):c.140T>C (p.Leu47Pro)	rs1271250198
NM_004700.4(KCNQ4):c.261_269del (p.Tyr88_Val90del)	rs1557977732
NM_004700.4(KCNQ4):c.796G>T (p.Asp266Tyr)	rs1558014576
NM_144498.4(OSBPL2):c.180_181del (p.His60fs)	rs1981202197

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