Variants with conflicting interpretations "uncertain significance" from Division of Medical Genetics, University of Washington and "likely benign" from any submitter

Minimum review status of the submission from Division of Medical Genetics, University of Washington:		Collection method of the submission from Division of Medical Genetics, University of Washington:
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: 10

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HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.26G>C (p.Cys9Ser)	rs140825795	0.00037
NM_001048174.2(MUTYH):c.850-2A>G	rs77542170	0.00035
NM_024675.4(PALB2):c.656A>G (p.Asp219Gly)	rs45594034	0.00021
NM_004360.5(CDH1):c.2644G>A (p.Asp882Asn)	rs200104963	0.00009
NM_000546.6(TP53):c.1015G>A (p.Glu339Lys)	rs17882252	0.00006
NM_007194.4(CHEK2):c.1556G>T (p.Arg519Leu)	rs587780180	0.00006
NM_000251.3(MSH2):c.1681G>A (p.Glu561Lys)	rs63750328	0.00002
NM_058216.3(RAD51C):c.746G>A (p.Arg249His)	rs730881925	0.00002
NM_000251.3(MSH2):c.2048G>T (p.Gly683Val)	rs755920849	0.00001
NM_000546.6(TP53):c.245C>T (p.Pro82Leu)	rs534447939	0.00001

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