Variants with conflicting interpretations "pathogenic" from Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research and "likely 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.4096+1G>A	rs80358178	0.00001
NM_000059.4(BRCA2):c.316+5G>A	rs81002840
NM_000059.4(BRCA2):c.6466_6469del (p.Ser2156fs)	rs80359596
NM_000059.4(BRCA2):c.6643del (p.Tyr2215fs)	rs80359614
NM_000059.4(BRCA2):c.9004G>A (p.Glu3002Lys)	rs80359152
NM_177438.3(DICER1):c.2987+1G>A	rs1555370248
NM_177438.3(DICER1):c.5138A>T (p.Asp1713Val)	rs1595331224
NM_177438.3(DICER1):c.904-1G>C	rs1566803555

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