ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.8611G>C (p.Glu2871Gln) (rs587782860)

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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 RCV000132479 SCV000187573 uncertain significance Hereditary cancer-predisposing syndrome 2014-04-15 criteria provided, single submitter clinical testing Insufficient or conflicting evidence
Clinical Genomics Lab,St. Jude Children's Research Hospital RCV000761078 SCV000890993 uncertain significance Acute myeloid leukemia 2016-06-10 no assertion criteria provided clinical testing

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