ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.68_316del249 (p.Asp23_Leu105del) (rs1555280328)

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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 RCV000502741 SCV000592323 likely pathogenic Hereditary breast and ovarian cancer syndrome criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000758982 SCV000887973 pathogenic not provided 2018-02-04 criteria provided, single submitter clinical testing

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