ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.63A>G (p.Lys21=) (rs1280004443)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
3DMed Clinical Laboratory Inc RCV000677832 SCV000803992 uncertain significance Neoplasm of the breast 2017-04-21 no assertion criteria provided clinical testing
Invitae RCV000527263 SCV000635506 likely benign Hereditary breast and ovarian cancer syndrome 2017-07-25 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000506652 SCV000600699 uncertain significance not specified 2016-12-06 criteria provided, single submitter clinical testing

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