ClinVar Miner

Submissions for variant NM_000038.6(APC):c.2484T>C (p.Thr828=)

dbSNP: rs1765192603
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001189569 SCV001356880 likely benign Hereditary cancer-predisposing syndrome 2019-08-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV004570393 SCV001636393 likely benign Familial adenomatous polyposis 1 2020-09-17 criteria provided, single submitter clinical testing

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