Variants with conflicting interpretations "likely benign" from 3DMed Clinical Laboratory Inc and "benign" from any submitter

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.1568A>G (p.His523Arg)	rs80358443	0.00009
NM_007294.4(BRCA1):c.811G>A (p.Val271Met)	rs80357244	0.00003

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