ClinVar for MedGen (Select 358118) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 374105	NM_000038.6(APC):c.4901del (p.Pro1634fs)	APC (P1351fs +12 more)	Deletion (frameshift variant)	Familial adenomatous polyposis 1 +2 more	GPathogenic
Select item 816	NM_000038.6(APC):c.3927_3931del (p.Glu1309fs)	APC (E1149fs +12 more)	Microsatellite (frameshift variant)	Familial adenomatous polyposis 1	GPathogenic FDA Recognized database