List of variants reported as likely benign for Autosomal recessive nonsyndromic hearing loss 1A by Illumina Laboratory Services, Illumina

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_004004.6(GJB2):c.*1197T>A	rs11841182	0.04451
NM_004004.6(GJB2):c.-15C>T	rs72561725	0.01589
NM_004004.6(GJB2):c.-216T>G	rs574815423	0.01243
NM_004004.6(GJB2):c.457G>A (p.Val153Ile)	rs111033186	0.00247
NM_004004.6(GJB2):c.249C>G (p.Phe83Leu)	rs111033218	0.00150
NM_004004.6(GJB2):c.380G>A (p.Arg127His)	rs111033196	0.00143
NM_004004.6(GJB2):c.478G>A (p.Gly160Ser)	rs34988750	0.00107
NM_004004.6(GJB2):c.11G>A (p.Gly4Asp)	rs111033222	0.00059
NM_004004.6(GJB2):c.*1C>T	rs111033327	0.00045
NM_004004.6(GJB2):c.355G>A (p.Glu119Lys)	rs150529554	0.00016
NM_004004.6(GJB2):c.241C>G (p.Leu81Val)	rs145216882	0.00015
NM_004004.6(GJB2):c.368C>A (p.Thr123Asn)	rs111033188	0.00014
NM_004004.6(GJB2):c.120A>C (p.Ala40=)	rs561870637	0.00012
NM_004004.6(GJB2):c.493C>T (p.Arg165Trp)	rs376898963	0.00006
NM_004004.6(GJB2):c.546G>A (p.Val182=)	rs752236261	0.00001

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