ClinVar Miner

Submissions for variant NM_001379150.1(IRS4):c.2635C>G (p.His879Asp)

dbSNP: rs1801164
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001730979 SCV001980736 benign Hypothyroidism, congenital, nongoitrous, 9 2021-08-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004714295 SCV005276498 benign not provided criteria provided, single submitter not provided
Clinical Genetics, Academic Medical Center RCV001700908 SCV001925891 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001700908 SCV001932219 benign not specified 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.