ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.6448A>C (p.Lys2150Gln) (rs1403648108)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000565008 SCV000665141 uncertain significance Hereditary cancer-predisposing syndrome 2017-08-07 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient evidence,In silico models in agreement (benign)
Counsyl RCV000662567 SCV000785170 uncertain significance Breast-ovarian cancer, familial 2 2017-05-19 criteria provided, single submitter clinical testing

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