Variants with conflicting interpretations "likely pathogenic" from Center for Precision Medicine, Meizhou People's Hospital and "pathogenic" from any submitter

Minimum review status of the submission from Center for Precision Medicine, Meizhou People's Hospital:		Collection method of the submission from Center for Precision Medicine, Meizhou People's Hospital:
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.8331+1G>A	rs81002837
NM_000059.4(BRCA2):c.8954-5A>G	rs886040949

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