ClinVar Miner

Submissions for variant NM_177438.3(DICER1):c.2041-91A>G

gnomAD frequency: 0.18396  dbSNP: rs2297730
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breakthrough Genomics, Breakthrough Genomics RCV000836370 SCV005293418 benign not provided criteria provided, single submitter not provided
GeneDx RCV000836370 SCV000978214 benign not provided 2018-06-16 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.

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