ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1287A>T (p.Pro429=)

dbSNP: rs2149783796
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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 RCV004571004 SCV001643436 likely benign Familial adenomatous polyposis 1 2019-05-29 criteria provided, single submitter clinical testing

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