Variants with conflicting interpretations "likely pathogenic" from CZECANCA consortium and "pathogenic" from any submitter

Minimum review status of the submission from CZECANCA consortium:		Collection method of the submission from CZECANCA consortium:
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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.7630-2A>C	rs587779866	0.00001
NM_000546.6(TP53):c.711G>A (p.Met237Ile)	rs587782664	0.00001
NM_058216.3(RAD51C):c.905-2_905-1del	rs587781995	0.00001
NM_007294.4(BRCA1):c.5074+3A>G	rs80358181
NM_058216.3(RAD51C):c.1026+5_1026+7del	rs587781410

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