ClinVar Miner

Submissions for variant NM_005045.4(RELN):c.9531C>T (p.Ala3177=)

gnomAD frequency: 0.00002  dbSNP: rs750621529
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
Genetic Services Laboratory, University of Chicago RCV000193324 SCV000248714 uncertain significance not specified 2014-06-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001435659 SCV001638485 likely benign Norman-Roberts syndrome; Familial temporal lobe epilepsy 7 2023-05-15 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.