ClinVar Miner

Submissions for variant NM_177438.3(DICER1):c.1753-43G>A

gnomAD frequency: 0.00160  dbSNP: rs74899136
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268548 SCV002551552 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing
GeneDx RCV001652428 SCV001869638 benign not provided 2018-10-02 criteria provided, single submitter clinical testing

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