ClinVar Miner

Submissions for variant NM_001356.5(DDX3X):c.3G>T (p.Met1Ile)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota RCV003992865 SCV004809336 pathogenic Intellectual disability, X-linked 102 2024-01-24 criteria provided, single submitter clinical testing

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