Variants with conflicting interpretations "pathogenic" from Cancer Variant Interpretation Group UK, Institute of Cancer Research, London and "uncertain significance" from any submitter

Minimum review status of the submission from Cancer Variant Interpretation Group UK, Institute of Cancer Research, London:		Collection method of the submission from Cancer Variant Interpretation Group UK, Institute of Cancer Research, London:
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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.8524C>T (p.Arg2842Cys)	rs80359104	0.00001
NM_000546.6(TP53):c.646G>A (p.Val216Met)	rs730882025
NM_007294.4(BRCA1):c.4357+6T>C	rs80358143

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