ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.68-17A>G

gnomAD frequency: 0.00001  dbSNP: rs1060504621
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000470680 SCV000560434 likely benign Hereditary breast ovarian cancer syndrome 2023-10-22 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000581854 SCV000688999 likely benign Hereditary cancer-predisposing syndrome 2017-10-24 criteria provided, single submitter clinical testing
GeneDx RCV001618709 SCV001847349 benign not provided 2015-09-08 criteria provided, single submitter clinical testing
Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute RCV001618709 SCV001906458 likely benign not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001618709 SCV001959315 likely benign not provided no assertion criteria provided clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001618709 SCV002037067 likely benign not provided no assertion criteria provided clinical testing

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