Variants with conflicting interpretations "uncertain significance" from 3DMed Clinical Laboratory Inc and "likely benign" from Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum review status of the submission from 3DMed Clinical Laboratory Inc:		Collection method of the submission from 3DMed Clinical Laboratory Inc:
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_000059.4(BRCA2):c.6325G>A (p.Val2109Ile)	rs79456940	0.00006
NM_000059.4(BRCA2):c.7522G>A (p.Gly2508Ser)	rs80358978	0.00004

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