ClinVar Miner

Submissions for variant NM_000038.6(APC):c.3879A>C (p.Thr1293=)

dbSNP: rs2149901126
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003771428 SCV001655965 likely benign Familial adenomatous polyposis 1 2022-07-27 criteria provided, single submitter clinical testing

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