ClinVar Miner

Submissions for variant NM_000038.6(APC):c.835-24A>T

gnomAD frequency: 0.00091  dbSNP: rs200399868
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000987554 SCV001136878 likely benign Familial adenomatous polyposis 1 2019-05-28 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV000987554 SCV004015792 likely benign Familial adenomatous polyposis 1 2023-07-07 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV000201972 SCV004025033 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000201972 SCV000257035 likely benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001723773 SCV001957175 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000201972 SCV001972307 benign not specified no assertion criteria provided clinical testing

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