ClinVar Miner

Submissions for variant NM_177438.3(DICER1):c.2437-113A>T

gnomAD frequency: 0.03006  dbSNP: rs57932364
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 RCV001612016 SCV005293415 benign not provided criteria provided, single submitter not provided
GeneDx RCV001612016 SCV001837995 benign not provided 2018-07-14 criteria provided, single submitter clinical testing

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