Variants with conflicting interpretations "pathogenic" from ClinGen InSiGHT Hereditary Colorectal Cancer/Polyposis Variant Curation Expert Panel and "likely pathogenic" from any submitter

Minimum review status of the submission from ClinGen InSiGHT Hereditary Colorectal Cancer/Polyposis Variant Curation Expert Panel:		Collection method of the submission from ClinGen InSiGHT Hereditary Colorectal Cancer/Polyposis Variant Curation Expert Panel:
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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.3927_3931del (p.Glu1309fs)	rs121913224
NM_000038.6(APC):c.532-8G>A	rs1060503323
Single allele

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