ClinVar Miner

Submissions for variant NM_000038.6(APC):c.245dup (p.Gly84fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
National Molecular Genetics Centre of Cancer Research, N.N. Alexandrov National Cancer Centre of Belarus RCV004577428 SCV005061400 pathogenic Familial adenomatous polyposis 1 2023-09-20 criteria provided, single submitter clinical testing

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