List of variants reported as uncertain significance for autosomal recessive nonsyndromic hearing loss 1A by Natera, Inc.

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Total variants: 31

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HGVS	dbSNP	gnomAD frequency
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.670A>C (p.Lys224Gln)	rs111033194	0.00015
NM_004004.6(GJB2):c.511G>A (p.Ala171Thr)	rs201004645	0.00014
NM_004004.6(GJB2):c.37G>A (p.Val13Met)	rs768130937	0.00010
NM_004004.6(GJB2):c.425T>C (p.Phe142Ser)	rs116769964	0.00007
NM_004004.6(GJB2):c.-22-18T>A	rs778602324	0.00005
NM_004004.6(GJB2):c.385G>A (p.Glu129Lys)	rs397516875	0.00004
NM_004004.6(GJB2):c.587T>C (p.Ile196Thr)	rs765172751	0.00004
NM_004004.6(GJB2):c.663G>C (p.Lys221Asn)	rs375599392	0.00004
NM_004004.6(GJB2):c.-7G>A	rs398123813	0.00003
NM_004004.6(GJB2):c.476A>T (p.Asp159Val)	rs28931592	0.00003
NM_004004.6(GJB2):c.488T>C (p.Met163Thr)	rs1273330603	0.00003
NM_004004.6(GJB2):c.677T>G (p.Val226Gly)	rs773846324	0.00002
NM_004004.6(GJB2):c.*4A>G	rs745748793	0.00001
NM_004004.6(GJB2):c.-22-7T>C	rs372197957	0.00001
NM_004004.6(GJB2):c.146C>T (p.Ala49Val)	rs1057517976	0.00001
NM_004004.6(GJB2):c.14C>T (p.Thr5Met)	rs781085903	0.00001
NM_004004.6(GJB2):c.188T>C (p.Val63Ala)	rs727504309	0.00001
NM_004004.6(GJB2):c.331A>G (p.Ile111Val)	rs1003660637	0.00001
NM_004004.6(GJB2):c.358G>A (p.Glu120Lys)	rs528216023	0.00001
NM_004004.6(GJB2):c.490C>G (p.Gln164Glu)	rs757699303	0.00001
NM_004004.6(GJB2):c.566C>A (p.Thr189Asn)	rs199790409	0.00001
NM_004004.6(GJB2):c.-16C>T	rs759745271
NM_004004.6(GJB2):c.-263C>G	rs1593353804
NM_004004.6(GJB2):c.100A>T (p.Met34Leu)	rs564084861
NM_004004.6(GJB2):c.187G>T (p.Val63Leu)	rs370696868
NM_004004.6(GJB2):c.284T>C (p.Val95Ala)	rs1250849257
NM_004004.6(GJB2):c.322A>G (p.Lys108Glu)	rs1959059283
NM_004004.6(GJB2):c.380G>T (p.Arg127Leu)	rs111033196
NM_004004.6(GJB2):c.445G>A (p.Ala149Thr)	rs111033225

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