ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.4312G>A (p.Val1438Ile) (rs786202874)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000165922 SCV000216677 uncertain significance Hereditary cancer-predisposing syndrome 2016-06-13 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient or conflicting evidence
Counsyl RCV000411249 SCV000489671 uncertain significance Breast-ovarian cancer, familial 2 2016-11-02 criteria provided, single submitter clinical testing
3DMed Clinical Laboratory Inc RCV000677852 SCV000804012 uncertain significance Neoplasm of the breast 2017-12-20 no assertion criteria provided clinical testing

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