ClinVar Miner

Submissions for variant NM_177438.3(DICER1):c.573+116C>T

gnomAD frequency: 0.10094  dbSNP: rs1953535
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
Breakthrough Genomics, Breakthrough Genomics RCV001652686 SCV005293425 benign not provided criteria provided, single submitter not provided
GeneDx RCV001652686 SCV001865846 benign not provided 2018-06-21 criteria provided, single submitter clinical testing

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