ClinVar Miner

Submissions for variant NM_177438.3(DICER1):c.3094-53del

dbSNP: rs371156380
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001708365 SCV001934746 benign not provided 2019-08-13 criteria provided, single submitter clinical testing

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