ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.7618-21G>T (rs376957350)

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Total submissions: 3
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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 RCV000500596 SCV000592130 uncertain significance not specified 2012-11-14 criteria provided, single submitter clinical testing
Mendelics RCV000144191 SCV001139188 benign Breast-ovarian cancer, familial 2 2019-05-28 criteria provided, single submitter clinical testing
Sharing Clinical Reports Project (SCRP) RCV000144191 SCV000189264 benign Breast-ovarian cancer, familial 2 2011-02-14 no assertion criteria provided clinical testing

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