ClinVar Miner

Submissions for variant NM_001356.5(DDX3X):c.904G>A (p.Gly302Ser)

dbSNP: rs875989802
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Human Genetics, University of Leuven RCV000211100 SCV000268065 likely pathogenic Intellectual disability, X-linked 102 2015-01-01 criteria provided, single submitter literature only

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