ClinVar Miner

Submissions for variant NM_001347721.2(DYRK1A):c.1762G>A (p.Ala588Thr) (rs200808105)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000711513 SCV000618133 likely benign not provided 2021-05-18 criteria provided, single submitter clinical testing
Invitae RCV000685711 SCV000813203 benign Mental retardation, autosomal dominant 7 2020-11-06 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000711513 SCV000841889 uncertain significance not provided 2019-06-04 criteria provided, single submitter clinical testing
Fulgent Genetics,Fulgent Genetics RCV000685711 SCV000895261 uncertain significance Mental retardation, autosomal dominant 7 2018-10-31 criteria provided, single submitter clinical testing

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