ClinVar Miner

Submissions for variant NM_000843.4(GRM6):c.1392A>G (p.Gly464=)

gnomAD frequency: 0.57251  dbSNP: rs11746675
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 5
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000179788 SCV000232095 benign not specified 2015-03-19 criteria provided, single submitter clinical testing
Invitae RCV000086026 SCV001723744 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV000086026 SCV001757198 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701503 SCV001934001 benign Congenital stationary night blindness 1B 2021-08-10 criteria provided, single submitter clinical testing
Retina International RCV000086026 SCV000118169 not provided not provided 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.