ClinVar Miner

Submissions for variant NM_000038.6(APC):c.4954del (p.Ser1652fs)

dbSNP: rs1554086327
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen RCV002292404 SCV002584912 pathogenic Familial adenomatous polyposis 1 2022-10-20 criteria provided, single submitter clinical testing

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