ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.1599+82_1599+84del

dbSNP: rs397515135
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
GeneDx RCV001546673 SCV001766231 likely benign not provided 2019-08-04 criteria provided, single submitter clinical testing
Tuberous sclerosis database (TSC2) RCV000055398 SCV000083619 not provided Tuberous sclerosis syndrome no assertion provided curation

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.