ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1008T>G (p.Ala336=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005124335 SCV005745277 likely benign Familial adenomatous polyposis 1 2024-03-12 criteria provided, single submitter clinical testing

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