List of variants reported as likely pathogenic for Autosomal recessive nonsyndromic hearing loss 1A by Integrating Genomics into Medicine, Frazer Institute, University Of Queensland

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_004004.6(GJB2):c.34G>T (p.Gly12Cys)	rs104894408	0.00009
NM_004004.6(GJB2):c.194A>G (p.Tyr65Cys)	rs111033203	0.00002
NM_004004.6(GJB2):c.583A>G (p.Met195Val)	rs532203068	0.00001
NM_004004.6(GJB2):c.458_475dup (p.Tyr158_Asp159insValPheTyrValMetTyr)

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