ClinVar Miner

Submissions for variant NM_001365276.2(TNXB):c.*163G>A

gnomAD frequency: 0.54891  dbSNP: rs1058152
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 RCV001619570 SCV001843605 benign not provided 2018-07-09 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002495970 SCV002802198 benign Ehlers-Danlos syndrome due to tenascin-X deficiency; Vesicoureteral reflux 8 2021-08-09 criteria provided, single submitter clinical testing

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.