ClinVar Miner

Submissions for variant GRCh38/hg38 2p22.3(chr2:32452646-33032447)x3

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA site 4 RCV000148094 SCV000190825 benign See cases 2011-08-12 criteria provided, single submitter clinical testing
ISCA site 4 RCV000050870 SCV000175325 benign See cases 2013-06-25 no assertion criteria provided clinical testing
ISCA site 1 RCV000050870 SCV000175326 conflicting data from submitters See cases 2011-08-05 no assertion criteria provided clinical testing Uncertain significance(6), Likely benign (3)

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.