ClinVar Miner

Submissions for variant NM_177438.3(DICER1):c.2040+54dup

dbSNP: rs141723381
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research RCV001200948 SCV001371897 likely benign not specified 2019-07-01 criteria provided, single submitter curation ACMG criteria met: BP2, BP4
GeneDx RCV001615141 SCV001833060 benign not provided 2018-06-23 criteria provided, single submitter clinical testing
Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research RCV001200948 SCV001371899 uncertain significance not specified 2019-07-01 flagged submission literature only

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