ClinVar Miner

Submissions for variant NM_001356.5(DDX3X):c.596G>A (p.Arg199His)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001255809 SCV003835476 uncertain significance Intellectual disability, X-linked 102 2022-08-31 criteria provided, single submitter clinical testing
Service de Génétique Moléculaire, Hôpital Robert Debré RCV001255809 SCV001432424 likely benign Intellectual disability, X-linked 102 no assertion criteria provided clinical testing

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