Variants with conflicting interpretations "pathogenic" from Molecular Genetics Laboratory, BC Children's and BC Women's Hospitals and "uncertain significance" from any submitter

Minimum review status of the submission from Molecular Genetics Laboratory, BC Children's and BC Women's Hospitals:		Collection method of the submission from Molecular Genetics Laboratory, BC Children's and BC Women's Hospitals:
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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001144967.3(NEDD4L):c.2677G>A (p.Glu893Lys)
NM_006087.4(TUBB4A):c.1172G>T (p.Arg391Leu)	rs886041021
NM_014639.4(SKIC3):c.2578-7_2578-3del	rs746874042

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