ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.-61C>T

gnomAD frequency: 0.00016  dbSNP: rs549332987
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000503514 SCV000593666 uncertain significance not specified 2016-07-28 criteria provided, single submitter clinical testing
Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute RCV001683526 SCV001905765 likely benign not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001683526 SCV001956124 likely benign not provided no assertion criteria provided clinical testing

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