Variants with conflicting interpretations "uncertain significance" from Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research and "benign" from Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden

Minimum review status of the submission from Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research:		Collection method of the submission from Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research:
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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.8567A>C (p.Glu2856Ala)	rs11571747	0.00158
NM_000059.4(BRCA2):c.8149G>T (p.Ala2717Ser)	rs28897747	0.00127
NM_000059.4(BRCA2):c.1151C>T (p.Ser384Phe)	rs41293475	0.00074
NM_000059.4(BRCA2):c.4570T>G (p.Phe1524Val)	rs56386506	0.00004

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