Variants with conflicting interpretations "likely benign" from INGEBI, INGEBI / CONICET and "uncertain significance" from Molecular Genetics Laboratory, BC Children's and BC Women's Hospitals

Minimum review status of the submission from INGEBI, INGEBI / CONICET:		Collection method of the submission from INGEBI, INGEBI / CONICET:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 1

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HGVS	dbSNP	gnomAD frequency
NM_004004.6(GJB2):c.478G>A (p.Gly160Ser)	rs34988750	0.00107

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