Variants with conflicting interpretations "likely benign" from Claritas Genomics and "benign" from Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum review status of the submission from Claritas Genomics:		Collection method of the submission from Claritas Genomics:
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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001110556.2(FLNA):c.6742C>T (p.Leu2248=)	rs113510895	0.00698
NM_001110556.2(FLNA):c.4866C>T (p.Tyr1622=)	rs200835571	0.00065

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