ClinVar Miner

Submissions for variant NM_000038.6(APC):c.7401A>G (p.Pro2467=)

dbSNP: rs1290380033
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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 RCV004562864 SCV001702813 likely benign Familial adenomatous polyposis 1 2018-09-30 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004003248 SCV004825760 likely benign Classic or attenuated familial adenomatous polyposis 2023-08-15 criteria provided, single submitter clinical testing

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