ClinVar Miner

Submissions for variant NM_177438.3(DICER1):c.2651-14T>G

dbSNP: rs753857234
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden RCV003237604 SCV002010934 uncertain significance not provided 2021-11-03 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268571 SCV002551540 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003750873 SCV004405390 likely benign DICER1-related tumor predisposition 2023-09-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV003237604 SCV005194174 uncertain significance not provided criteria provided, single submitter not provided

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