ClinVar Miner

Submissions for variant NM_002485.5(NBN):c.702+84G>C

gnomAD frequency: 0.00405  dbSNP: rs104895036
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
National Health Laboratory Service, Universitas Academic Hospital and University of the Free State RCV002225315 SCV002505311 likely benign Hereditary breast ovarian cancer syndrome 2022-04-19 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003315629 SCV004016045 likely benign Acute lymphoid leukemia 2023-07-07 criteria provided, single submitter clinical testing
Harris Lab, University of Minnesota RCV000114879 SCV000148774 not provided not provided no assertion provided not provided
University of Washington Department of Laboratory Medicine, University of Washington RCV000209234 SCV000265318 likely benign Hereditary cancer-predisposing syndrome 2015-12-01 no assertion criteria provided clinical testing

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.