ClinVar Miner

Submissions for variant NM_000038.6(APC):c.2361T>C (p.Ser787=)

dbSNP: rs1339834096
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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 RCV004568862 SCV000647234 likely benign Familial adenomatous polyposis 1 2017-03-10 criteria provided, single submitter clinical testing

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