ClinVar Miner

Submissions for variant NM_017637.6(BNC2):c.84A>T (p.Ala28=)

gnomAD frequency: 0.02974  dbSNP: rs76485966
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
Invitae RCV002055270 SCV002327015 benign not provided 2024-01-20 criteria provided, single submitter clinical testing
Centre for molecular medicine, Karolinska Institutet RCV000190271 SCV000143812 not provided Hypotension no assertion provided not provided

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.