ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.2623G>A (p.Val875Ile) (rs587782582)

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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 RCV000131916 SCV000186971 uncertain significance Hereditary cancer-predisposing syndrome 2017-10-04 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient or conflicting evidence
CeGaT Praxis fuer Humangenetik Tuebingen RCV000512784 SCV000608678 likely benign not provided 2017-06-30 criteria provided, single submitter clinical testing

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