Variants with conflicting interpretations "pathogenic" from University Health Network, Princess Margaret Cancer Centre and "likely pathogenic" from any submitter

Minimum review status of the submission from University Health Network, Princess Margaret Cancer Centre:		Collection method of the submission from University Health Network, Princess Margaret 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.733G>A (p.Gly245Ser)	rs28934575	0.00001
NM_004985.5(KRAS):c.35G>A (p.Gly12Asp)	rs121913529	0.00001
NM_000546.6(TP53):c.380C>T (p.Ser127Phe)	rs730881999
NM_000546.6(TP53):c.742C>T (p.Arg248Trp)	rs121912651
NM_000546.6(TP53):c.818G>A (p.Arg273His)	rs28934576
Single allele

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