Variants with conflicting interpretations "likely benign" from Cancer Genetics Laboratory, Peter MacCallum Cancer Centre and "uncertain significance" from any submitter

Minimum review status of the submission from Cancer Genetics Laboratory, Peter MacCallum Cancer Centre:		Collection method of the submission from Cancer Genetics Laboratory, Peter MacCallum Cancer Centre:
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: 7

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HGVS	dbSNP	gnomAD frequency
NM_024675.4(PALB2):c.1194G>A (p.Val398=)	rs61755173	0.00103
NM_024675.4(PALB2):c.232G>A (p.Val78Ile)	rs515726085	0.00013
NM_024675.4(PALB2):c.2379C>T (p.Gly793=)	rs377626805	0.00009
NM_024675.4(PALB2):c.1189A>T (p.Thr397Ser)	rs367578415	0.00003
NM_024675.4(PALB2):c.94C>G (p.Leu32Val)	rs151316635	0.00003
NM_024675.4(PALB2):c.1478C>T (p.Pro493Leu)	rs770965402
NM_024675.4(PALB2):c.508A>G (p.Arg170Gly)	rs864622622

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