ClinVar Miner

Submissions for variant NM_001111125.3(IQSEC2):c.363C>T (p.Gly121=)

gnomAD frequency: 0.00001  dbSNP: rs1178634147
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 RCV001916756 SCV002191705 likely benign Intellectual disability, X-linked 1 2024-06-28 criteria provided, single submitter clinical testing
GeneDx RCV004719200 SCV005325941 uncertain significance not provided 2023-07-28 criteria provided, single submitter clinical testing Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this variant does not alter splicing; Has not been previously published as pathogenic or benign to our knowledge

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.