ClinVar Miner

Submissions for variant NM_000038.6(APC):c.4728dup (p.Glu1577fs)

dbSNP: rs2149922239
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
University of Science and Technology Houari Boumediene, Laboratory of Molecular and Cellular Biology (LBCM) RCV001843389 SCV002102506 pathogenic Familial adenomatous polyposis 1 criteria provided, single submitter clinical testing

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