Variants with conflicting interpretations "pathogenic" from Sharing Clinical Reports Project (SCRP) and "likely benign" from any submitter

Minimum review status of the submission from Sharing Clinical Reports Project (SCRP):		Collection method of the submission from Sharing Clinical Reports Project (SCRP):
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.5428G>A (p.Val1810Ile)	rs80358766	0.00002
NM_007294.4(BRCA1):c.5363G>A (p.Gly1788Asp)	rs80357069

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