ClinVar Miner

Submissions for variant NM_000038.6(APC):c.2166T>C (p.Ser722=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004803701 SCV005425753 likely benign Classic or attenuated familial adenomatous polyposis 2024-02-22 criteria provided, single submitter clinical testing

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