List of variants in gene APC reported as benign for adenocarcinoma

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.4479G>A (p.Thr1493=)	rs41115	0.59177
NM_000038.6(APC):c.1458T>C (p.Tyr486=)	rs2229992	0.46792
NM_000038.6(APC):c.4326T>A (p.Pro1442=)	rs67622085	0.00705

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