ClinVar Miner

Submissions for variant NM_001347721.2(DYRK1A):c.1363C>G (p.Pro455Ala)

dbSNP: rs756860738
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001034138 SCV001197463 likely benign DYRK1A-related intellectual disability syndrome 2019-10-25 criteria provided, single submitter clinical testing

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