ClinVar Miner

Submissions for variant NM_000038.6(APC):c.646-15C>A

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV004574170 SCV004382749 likely benign Familial adenomatous polyposis 1 2025-01-22 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004011658 SCV004827799 likely benign Classic or attenuated familial adenomatous polyposis 2023-08-15 criteria provided, single submitter clinical testing

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