Variants with conflicting interpretations "likely pathogenic" from ClinGen TP53 Variant Curation Expert Panel, ClinGen and "pathogenic" from Labcorp Genetics (formerly Invitae), Labcorp

Minimum review status of the submission from ClinGen TP53 Variant Curation Expert Panel, ClinGen:		Collection method of the submission from ClinGen TP53 Variant Curation Expert Panel, ClinGen:
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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000546.6(TP53):c.1031T>C (p.Leu344Pro)	rs121912662
NM_000546.6(TP53):c.482_487del (p.Ala161_Tyr163delinsAsp)	rs2073376974
NM_000546.6(TP53):c.524G>T (p.Arg175Leu)	rs28934578
NM_000546.6(TP53):c.538G>A (p.Glu180Lys)	rs879253911
NM_000546.6(TP53):c.569C>T (p.Pro190Leu)	rs876660825

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