ClinVar Miner

Submissions for variant NM_001356.5(DDX3X):c.165dup (p.Asp56fs)

dbSNP: rs2147348607
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
Laboratoire Génétique Moléculaire, CHRU TOURS RCV001541937 SCV001760569 pathogenic not provided 2020-02-22 criteria provided, single submitter clinical testing

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