ClinVar Miner

Submissions for variant NM_001356.4(DDX3X):c.1126C>T (p.Arg376Cys) (rs796052231)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000190550 SCV000245431 pathogenic Mental retardation, X-linked 102 2015-08-06 no assertion criteria provided literature only
Dobyns Lab,Seattle Children's Research Institute RCV000190550 SCV000916339 pathogenic Mental retardation, X-linked 102 2019-02-18 no assertion criteria provided research

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