ClinVar Miner

Submissions for variant GRCh38/hg38 15q13.3(chr15:31806467-32134668)x3

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
ISCA site 4 RCV000141257 SCV000182157 benign See cases 2010-03-30 no assertion criteria provided clinical testing
ISCA site 1 RCV000141257 SCV000182158 conflicting data from submitters See cases 2013-04-04 no assertion criteria provided clinical testing Uncertain significance(1), Likely benign (1)

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.