ClinVar Miner

Submissions for variant NM_003410.4(ZFX):c.2321A>G (p.Tyr774Cys)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Undiagnosed Diseases Network, NIH RCV003991066 SCV005889623 pathogenic Intellectual developmental disorder, x-linked, syndromic 37 2024-07-02 criteria provided, single submitter clinical testing
OMIM RCV003991066 SCV004808372 pathogenic Intellectual developmental disorder, x-linked, syndromic 37 2024-04-02 no assertion criteria provided literature only

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.