ClinVar Miner

Submissions for variant NM_201525.4(ADGRG1):c.1356G>A (p.Thr452=)

gnomAD frequency: 0.00035  dbSNP: rs151020094
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000593804 SCV000709258 uncertain significance not provided 2017-06-09 criteria provided, single submitter clinical testing
Invitae RCV000593804 SCV001071080 likely benign not provided 2024-01-25 criteria provided, single submitter clinical testing
GeneDx RCV000593804 SCV001987173 uncertain significance not provided 2019-12-30 criteria provided, single submitter clinical testing Has not been previously published as pathogenic or benign to our knowledge

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.