Variants in gene GJB1 with conflicting interpretations "pathogenic" and "likely benign"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

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HGVS	dbSNP	gnomAD frequency
NM_000166.6(GJB1):c.704T>G (p.Phe235Cys)	rs104894825	0.00295
NM_000166.6(GJB1):c.688C>T (p.Arg230Cys)	rs587781246	0.00014
NM_000166.6(GJB1):c.*15C>T	rs1057520778

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