ClinVar Miner

Submissions for variant NM_000089.3(COL1A2):c.96+10C>T (rs185341110)

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
GeneDx RCV001698182 SCV000531137 likely benign not provided 2018-05-04 criteria provided, single submitter clinical testing
Invitae RCV000865374 SCV001006327 benign Osteogenesis imperfecta type I; Ehlers-Danlos syndrome, classic type I 2020-11-25 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001285358 SCV001471775 benign none provided 2020-08-24 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.