ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.3403-34T>A

gnomAD frequency: 0.01280  dbSNP: rs148368017
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001663087 SCV001872407 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
National Health Laboratory Service, Universitas Academic Hospital and University of the Free State RCV002225899 SCV002504696 likely benign Hereditary breast ovarian cancer syndrome 2022-04-19 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV001694148 SCV002760554 benign not specified 2025-03-04 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001663087 SCV005216412 likely benign not provided criteria provided, single submitter not provided
Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute RCV001694148 SCV001906362 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001694148 SCV001952300 benign not specified no assertion criteria provided clinical testing
Natera, Inc. RCV001827555 SCV002080363 benign Ataxia-telangiectasia syndrome 2019-10-17 no assertion criteria provided clinical testing

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