Variants in gene GJB1 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000166.6(GJB1):c.235C>T (p.Leu79=)	rs144717157	0.00186
NM_000166.6(GJB1):c.688C>T (p.Arg230Cys)	rs587781246	0.00014

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