List of variants in gene GJB2 reported as likely pathogenic for Nonsyndromic hearing loss and deafness

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP
NM_004004.6(GJB2):c.-22-2A>C	rs201895089
NM_004004.6(GJB2):c.-23G>T	rs786204734
NM_004004.6(GJB2):c.110T>C (p.Val37Ala)	rs141774369
NM_004004.6(GJB2):c.227T>C (p.Leu76Pro)	rs111033361
NM_004004.6(GJB2):c.2T>C (p.Met1Thr)	rs371086981
NM_004004.6(GJB2):c.326G>T (p.Gly109Val)
NM_004004.6(GJB2):c.34G>T (p.Gly12Cys)	rs104894408
NM_004004.6(GJB2):c.563A>G (p.Lys188Arg)	rs1131691709
NM_004004.6(GJB2):c.583A>G (p.Met195Val)	rs532203068
NM_004004.6(GJB2):c.632G>A (p.Cys211Tyr)

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