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: 4
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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 RCV003316775 SCV004015914 benign Familial adenomatous polyposis 1 2023-07-07 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000583366 SCV000691707 benign not specified no assertion criteria provided clinical testing

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