ClinVar Miner

Submissions for variant NM_000038.6(APC):c.4653A>G (p.Lys1551=)

dbSNP: rs2149920153
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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 RCV004570996 SCV001620764 likely benign Familial adenomatous polyposis 1 2020-05-15 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004006949 SCV004822951 likely benign Classic or attenuated familial adenomatous polyposis 2023-04-03 criteria provided, single submitter clinical testing

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