ClinVar Miner

Submissions for variant NM_000629.3(IFNAR1):c.624G>A (p.Thr208=)

gnomAD frequency: 0.00177  dbSNP: rs144040431
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 RCV001520724 SCV001729899 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001520724 SCV004153112 likely benign not provided 2022-09-01 criteria provided, single submitter clinical testing IFNAR1: BP4, BP7

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.