List of variants in gene GJB3 reported as pathogenic for autosomal dominant nonsyndromic hearing loss

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_024009.3(GJB3):c.547G>A (p.Glu183Lys)	rs74315318	0.00019
NM_024009.3(GJB3):c.538C>T (p.Arg180Ter)	rs74315319	0.00003
NM_024009.3(GJB3):c.101T>C (p.Leu34Pro)	rs28937583

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