Variants with conflicting interpretations "likely pathogenic" from Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research and "pathogenic" from any submitter

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:
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: 8

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.4986+6T>C	rs80358086	0.00001
NM_000059.4(BRCA2):c.6938-2A>G	rs81002863
NM_007294.4(BRCA1):c.4675+1G>A	rs80358044
NM_177438.3(DICER1):c.2516C>T (p.Ser839Phe)	rs387906934
NM_177438.3(DICER1):c.4748T>G (p.Leu1583Arg)	rs137852976
NM_177438.3(DICER1):c.5123G>A (p.Gly1708Glu)	rs886037724
NM_177438.3(DICER1):c.5465A>T (p.Asp1822Val)	rs886037729
NM_177438.3(DICER1):c.735-1_741delinsA	rs886037731

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