List of variants in gene APC reported as pathogenic by ClinGen InSiGHT Hereditary Colorectal Cancer/Polyposis Variant Curation Expert Panel

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.1311_1312+1del	rs397514030
NM_000038.6(APC):c.1900dup (p.Ser634fs)
NM_000038.6(APC):c.3927_3931del (p.Glu1309fs)	rs121913224
NM_000038.6(APC):c.4778del (p.Lys1593fs)	rs1554086185
NM_000038.6(APC):c.509_512del (p.Asp170fs)	rs387906231
NM_000038.6(APC):c.532-8G>A	rs1060503323
NM_000038.6(APC):c.847C>T (p.Arg283Ter)	rs786201856

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