ClinVar Miner

Submissions for variant NCBI36/hg18 Xq27.2(chrX:140180787-140591819)x1

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
ISCA site 19 RCV000450849 SCV000494794 benign/likely benign See cases no assertion criteria provided clinical testing Likely benign (1), Benign (2)

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.