ClinVar Miner

Submissions for variant NM_000038.6(APC):c.3905del (p.Leu1302fs)

dbSNP: rs2149901744
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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) RCV001845059 SCV002104261 pathogenic Familial adenomatous polyposis 1 criteria provided, single submitter clinical testing

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