ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1636A>G (p.Ser546Gly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine, Sinai Health System RCV005360440 SCV005917838 uncertain significance Classic or attenuated familial adenomatous polyposis 2021-05-19 criteria provided, single submitter clinical testing

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