ClinVar Miner

Submissions for variant NM_001347721.2(DYRK1A):c.637+4A>T

dbSNP: rs2052877663
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Diagnostic Laboratory, Strasbourg University Hospital RCV001260678 SCV001437770 likely benign Intellectual disability 2020-09-10 criteria provided, single submitter clinical testing

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