ClinVar Miner

Submissions for variant GRCh37/hg19 16p12.2(chr16:21801889-22431357)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
ARUP Laboratories, Cytogenetics and Genomic Microarray,ARUP Laboratories RCV000448291 SCV000502969 uncertain significance See cases no assertion criteria provided clinical testing
ISCA site 1 RCV000511874 SCV000586678 conflicting data from submitters See cases 2016-02-29 no assertion criteria provided clinical testing Uncertain significance(2), Likely benign (1)
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000683789 SCV000811298 uncertain significance not provided 2019-05-09 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.