ClinVar Miner

Submissions for variant NM_177438.2(DICER1):c.4050+1G>A (rs875989783)

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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 RCV000493490 SCV000581553 likely pathogenic Hereditary cancer-predisposing syndrome 2013-09-23 criteria provided, single submitter clinical testing
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine RCV000211099 SCV000267167 pathogenic Pineoblastoma 2014-07-15 criteria provided, single submitter research
PreventionGenetics RCV000851414 SCV000993695 likely pathogenic not provided 2014-04-17 criteria provided, single submitter clinical testing

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