ClinVar Miner

Submissions for variant NM_000038.6(APC):c.4083C>A (p.Pro1361=)

dbSNP: rs1464598628
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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 RCV003773902 SCV002449448 likely benign Familial adenomatous polyposis 1 2021-05-07 criteria provided, single submitter clinical testing

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