ClinVar Miner

Submissions for variant GRCh37/hg19 1p36.33-36.32(chr1:852863-4203509)x3

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Limoges University Hospital Laboratory,Limoges University Hospital RCV000519759 SCV000579220 pathogenic Distal trisomy 1p36 2016-03-25 no assertion criteria provided clinical testing 1p36.3 microduplication syndrome is the mirror of the 1p36.3 microdeletion syndrome, it involves many genes, of which several are likely causal of phenotypical features observed in the syndrome

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.