ClinVar Miner

Submissions for variant NM_001145661.2(GATA2):c.-5C>G (rs374415484)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000243386 SCV000306833 likely benign not specified criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000243386 SCV000594911 likely benign not specified 2016-09-29 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000984811 SCV001132692 likely benign not provided 2016-08-30 criteria provided, single submitter clinical testing
GeneDx RCV000984811 SCV001788863 likely benign not provided 2021-03-28 no assertion criteria provided clinical testing

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.