ClinVar Miner

Submissions for variant NM_000038.6(APC):c.2019T>C (p.Ser673=)

dbSNP: rs1580617579
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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 RCV004562854 SCV001686769 likely benign Familial adenomatous polyposis 1 2018-09-10 criteria provided, single submitter clinical testing

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