ClinVar Miner

Submissions for variant NM_001122769.3(LCA5):c.1083A>G (p.Pro361=)

gnomAD frequency: 0.00021  dbSNP: rs367733392
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 RCV001517478 SCV001725986 benign not provided 2024-11-05 criteria provided, single submitter clinical testing
Natera, Inc. RCV001280510 SCV001467694 uncertain significance Leber congenital amaurosis 2020-05-15 no assertion criteria provided 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.