ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.7617+39G>A (rs190660894)

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Total submissions: 2
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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 RCV000504280 SCV000592129 likely benign not specified 2017-10-25 criteria provided, single submitter clinical testing
Michigan Medical Genetics Laboratories,University of Michigan RCV000211042 SCV000196006 benign Breast-ovarian cancer, familial 2 2014-11-03 criteria provided, single submitter clinical testing

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