ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1409-26T>G

gnomAD frequency: 0.00005  dbSNP: rs9282598
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001540864 SCV001758792 likely benign not provided 2018-08-11 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268510 SCV002550583 benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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