ClinVar Miner

Submissions for variant GRCh38/hg38 22q11.23(chr22:23377984-24563859)x3

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
ISCA site 14 RCV000148169 SCV000190904 uncertain significance See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 17 RCV000148169 SCV000190905 uncertain significance See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 4 RCV000053179 SCV000175678 pathogenic See cases 2010-03-30 no assertion criteria provided clinical testing
ISCA site 1 RCV000053179 SCV000175679 uncertain significance See cases 2011-09-12 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.