ClinVar Miner

Submissions for variant NM_001347721.2(DYRK1A):c.450del (p.Arg149_Tyr150insTer)

dbSNP: rs2148582538
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Diagnostic Laboratory, Strasbourg University Hospital RCV001507303 SCV001712094 pathogenic Intellectual disability 2021-06-07 no assertion criteria provided clinical testing

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