ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.67+62T>G (rs11571574)

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Total submissions: 8
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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 RCV000503004 SCV000591656 likely benign not specified 2017-10-25 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000503004 SCV000602748 benign not specified 2017-05-01 criteria provided, single submitter clinical testing
Color Health, Inc RCV000582922 SCV000688994 benign Hereditary cancer-predisposing syndrome 2015-03-11 criteria provided, single submitter clinical testing
Invitae RCV001512186 SCV001719551 benign Hereditary breast and ovarian cancer syndrome 2020-12-06 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000113082 SCV000146097 uncertain significance Breast-ovarian cancer, familial 2 2010-12-17 no assertion criteria provided clinical testing
Clinical Genetics Laboratory, Department of Pathology,Netherlands Cancer Institute RCV000503004 SCV001905733 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000503004 SCV001930453 benign not specified no assertion criteria provided clinical testing
Human Genetics - Radboudumc,Radboudumc RCV001723675 SCV001955755 likely benign not provided no assertion criteria provided clinical testing

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