ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.67+13T>C

gnomAD frequency: 0.00001  dbSNP: rs1555280121
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000583948 SCV000688992 likely benign Hereditary cancer-predisposing syndrome 2016-05-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001503419 SCV001708274 likely benign Hereditary breast ovarian cancer syndrome 2024-02-02 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002222558 SCV002500662 likely benign not specified 2024-12-11 criteria provided, single submitter clinical testing

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