ClinVar Miner

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

gnomAD frequency: 0.00405  dbSNP: rs104895036
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Total submissions: 5
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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
Breakthrough Genomics, Breakthrough Genomics RCV000114879 SCV005221706 likely benign not provided criteria provided, single submitter not provided
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

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