ClinVar Miner

Submissions for variant NM_022336.4(EDAR):c.1024+16del

dbSNP: rs3833574
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000242704 SCV000314026 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV000143980 SCV001885570 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Invitae RCV002055860 SCV002339405 benign Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant; Autosomal recessive hypohidrotic ectodermal dysplasia syndrome 2024-01-29 criteria provided, single submitter clinical testing
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000143980 SCV000188866 unknown not provided no assertion criteria provided not provided Converted during submission to Uncertain significance.

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.