ClinVar Miner

Submissions for variant NM_004370.6(COL12A1):c.3257G>A (p.Arg1086Gln)

gnomAD frequency: 0.00002  dbSNP: rs757917876
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
Labcorp Genetics (formerly Invitae), Labcorp RCV003011097 SCV003299209 likely benign Ullrich congenital muscular dystrophy 2; Bethlem myopathy 2 2023-06-25 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003146719 SCV003833353 uncertain significance not provided 2022-03-03 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.