ClinVar Miner

Submissions for variant NM_000038.6(APC):c.729+23T>C

gnomAD frequency: 0.00381  dbSNP: rs75111475
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001557938 SCV001779790 likely benign not provided 2018-06-23 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV000583366 SCV002550571 benign not specified 2023-08-15 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV004562620 SCV004015914 benign Familial adenomatous polyposis 1 2023-07-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001557938 SCV005226780 likely benign not provided criteria provided, single submitter not provided
Mayo Clinic Laboratories, Mayo Clinic RCV000583366 SCV000691707 benign not specified no assertion criteria provided clinical testing

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