ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.1509+11T>C

gnomAD frequency: 0.00001  dbSNP: rs397517424
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
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000039534 SCV000063223 likely benign not specified 2012-09-22 criteria provided, single submitter clinical testing 1509+11T>C in intron 8 of GPR98: This variant is not expected to have clinical s ignificance because it is not located within the conserved region of the splice consensus sequence.
Invitae RCV003546464 SCV004265838 likely benign not provided 2023-07-09 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.