ClinVar Miner

Submissions for variant NM_001356.5(DDX3X):c.930dup (p.Arg311fs)

dbSNP: rs2147353994
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV001780614 SCV002018156 pathogenic Intellectual disability, X-linked 102 2019-06-18 criteria provided, single submitter clinical testing

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