ClinVar Miner

Submissions for variant NM_015021.3(ZNF292):c.6578A>C (p.Tyr2193Ser)

dbSNP: rs1554208945
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 RCV000626040 SCV000746655 likely pathogenic ZNF292-related neurodevelopmental condition 2017-10-24 criteria provided, single submitter clinical testing
University of Washington Center for Mendelian Genomics, University of Washington RCV001261762 SCV001439078 uncertain significance Neurodevelopmental disorder no assertion criteria provided research

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.