List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 1A by Myriad Genetics, Inc.

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_004004.6(GJB2):c.587T>C (p.Ile196Thr)	rs765172751	0.00003
NM_004004.6(GJB2):c.557C>T (p.Thr186Met)	rs753674300	0.00002
NM_004004.6(GJB2):c.585G>C (p.Met195Ile)	rs570552952	0.00002
NM_004004.6(GJB2):c.126G>T (p.Glu42Asp)	rs535635403	0.00001
NM_004004.6(GJB2):c.188T>C (p.Val63Ala)	rs727504309	0.00001
NM_004004.6(GJB2):c.475G>A (p.Asp159Asn)	rs373684994

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