ClinVar Miner

Submissions for variant NM_001347721.2(DYRK1A):c.300+7C>T (rs537532878)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000194947 SCV000247237 uncertain significance not specified 2014-08-20 criteria provided, single submitter clinical testing
Invitae RCV000977596 SCV001125515 likely benign not provided 2018-11-02 criteria provided, single submitter clinical testing
Invitae RCV001465882 SCV001669879 likely benign Mental retardation, autosomal dominant 7 2020-04-14 criteria provided, single submitter clinical testing

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