ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.9648+84G>A

gnomAD frequency: 0.00096  dbSNP: rs81002832
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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 RCV000045876 SCV000073889 benign Hereditary breast ovarian cancer syndrome 2024-11-05 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000114143 SCV000743526 likely benign Breast-ovarian cancer, familial, susceptibility to, 2 2017-07-28 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000114143 SCV000147687 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 2 2010-12-17 no assertion criteria provided clinical testing
Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute RCV001682748 SCV001905775 likely benign not provided no assertion criteria provided clinical testing

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