Variants with conflicting interpretations "uncertain significance" from Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute and "benign" from any submitter

Minimum review status of the submission from Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute:		Collection method of the submission from Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute:
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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000249.4(MLH1):c.1633A>G (p.Thr545Ala)	rs267607840	0.00004
NM_000059.4(BRCA2):c.9116C>T (p.Pro3039Leu)	rs80359167

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