ClinVar Miner

List of variants in gene APC reported as likely benign for Familial colorectal cancer

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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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.4360A>G (p.Lys1454Glu)	rs111866410	0.00271
NM_000038.6(APC):c.6857C>T (p.Ala2286Val)	rs200587641	0.00036

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