Variants with conflicting interpretations "pathogenic" from Counsyl and "risk factor" from any submitter

Minimum review status of the submission from Counsyl:		Collection method of the submission from Counsyl:
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: 4

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HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.556C>T (p.Arg186Ter)	rs387906843	0.00003
NM_000075.4(CDK4):c.70C>T (p.Arg24Cys)	rs11547328
NM_002878.4(RAD51D):c.757C>T (p.Arg253Ter)	rs137886232
NM_058216.3(RAD51C):c.397C>T (p.Gln133Ter)	rs387907159

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