ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.516+14del

dbSNP: rs1336445194
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine, Sinai Health System RCV000500284 SCV000591689 likely benign not specified criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000581900 SCV000688916 likely benign Hereditary cancer-predisposing syndrome 2017-07-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001403704 SCV001605582 likely benign Hereditary breast ovarian cancer syndrome 2024-05-01 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000500284 SCV004021063 uncertain significance not specified 2023-06-02 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV000500284 SCV004027395 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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