ClinVar Miner

Submissions for variant NM_000038.6(APC):c.221-29G>C

gnomAD frequency: 0.00025  dbSNP: rs369645686
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV000202081 SCV002550551 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316115 SCV004015881 likely benign Familial adenomatous polyposis 1 2023-07-07 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000202081 SCV000256947 likely benign not specified no assertion criteria provided research

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