List of variants reported as likely pathogenic for Autosomal recessive nonsyndromic hearing loss 1A by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_004004.6(GJB2):c.-22-2A>C	rs201895089	0.00056
NM_004004.6(GJB2):c.110T>C (p.Val37Ala)	rs141774369	0.00014
NM_004004.6(GJB2):c.34G>T (p.Gly12Cys)	rs104894408	0.00009
NM_004004.6(GJB2):c.298del (p.His100fs)	rs775828835	0.00002
NM_004004.6(GJB2):c.299A>T (p.His100Leu)	rs1422767764	0.00002
NM_000082.4(ERCC8):c.478G>A (p.Ala160Thr)	rs281875222	0.00001
NM_004004.6(GJB2):c.279G>A (p.Met93Ile)	rs397516871	0.00001
NM_004004.6(GJB2):c.11del (p.Gly4fs)	rs1555342014
NM_004004.6(GJB2):c.56G>C (p.Ser19Thr)	rs80338941
NM_004004.6(GJB2):c.592_600delinsCAGTGTTCATGACATTC (p.Val198_Gly200delinsGlnCysSerTer)	rs111033335

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