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

Minimum review status of the submission from GeneDx:		Collection method of the submission from GeneDx:
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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_007194.4(CHEK2):c.1312G>T (p.Asp438Tyr)	rs200050883	0.00034
NM_000051.4(ATM):c.4414T>G (p.Leu1472Val)	rs539676759	0.00009
NM_000059.4(BRCA2):c.7463G>A (p.Arg2488Lys)	rs80358968	0.00001
NM_000059.4(BRCA2):c.8417C>T (p.Ser2806Leu)	rs587782785	0.00001
NM_000059.4(BRCA2):c.9116C>T (p.Pro3039Leu)	rs80359167

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