ClinVar Miner

Submissions for variant NM_177438.2(DICER1):c.3334A>G (p.Asn1112Asp) (rs587778229)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000280432 SCV000389749 likely benign Pleuropulmonary blastoma 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000462299 SCV000553584 likely benign not provided 2019-01-14 criteria provided, single submitter clinical testing
Ambry Genetics RCV000562797 SCV000661855 uncertain significance Hereditary cancer-predisposing syndrome 2017-08-22 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient evidence
ITMI RCV000120638 SCV000084799 not provided not specified 2013-09-19 no assertion provided reference population

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