ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.7805+11C>A

gnomAD frequency: 0.00001  dbSNP: rs1060504610
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001088515 SCV000560390 likely benign Hereditary breast ovarian cancer syndrome 2025-01-23 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000581131 SCV000683907 likely benign Hereditary cancer-predisposing syndrome 2016-04-27 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV005239050 SCV000695102 likely benign not specified 2024-12-11 criteria provided, single submitter clinical testing
GeneDx RCV000586049 SCV001890341 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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