ClinVar Miner

Submissions for variant NM_005215.4(DCC):c.3073C>T (p.Arg1025Ter)

dbSNP: rs1909920586
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Medical Genetics, Medical University of Vienna RCV001645010 SCV001519076 pathogenic Mirror movements 1 2021-03-10 no assertion criteria provided clinical testing

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