ClinVar Miner

Submissions for variant NM_001195553.2(DCX):c.809-1G>A (rs587783589)

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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 RCV000145892 SCV000193029 pathogenic Heterotopia 2013-02-08 criteria provided, single submitter clinical testing
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000660394 SCV000782474 likely pathogenic Lissencephaly, X-linked 2016-06-30 criteria provided, single submitter clinical testing

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