ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.4968A>G (p.Thr1656=) (rs1060504597)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000466088 SCV000560439 likely benign not provided 2016-08-09 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000500689 SCV000591935 likely benign not specified 2014-04-16 criteria provided, single submitter clinical testing
Color RCV001183454 SCV001349182 likely benign Hereditary cancer-predisposing syndrome 2019-08-21 criteria provided, single submitter clinical testing
Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research RCV000735558 SCV000863696 likely benign Breast and/or ovarian cancer 2014-01-15 no assertion criteria provided clinical testing

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