ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.8953+98T>C (rs81002901)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000045670 SCV000073683 benign Hereditary breast and ovarian cancer syndrome 2016-03-27 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000504250 SCV000592238 benign not specified criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000114021 SCV000147498 not provided Breast-ovarian cancer, familial 2 no assertion provided clinical testing

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