ClinVar Miner

Submissions for variant NM_016222.4(DDX41):c.27+9G>A

dbSNP: rs765022870
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000502282 SCV000594332 uncertain significance not specified 2016-12-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003718247 SCV004514455 likely benign not provided 2023-02-23 criteria provided, single submitter clinical testing

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