ClinVar Miner

Submissions for variant NM_001127671.2(LIFR):c.143-37GT[13] (rs10637374)

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
Illumina Clinical Services Laboratory,Illumina RCV000308475 SCV000457602 uncertain significance Stüve-Wiedemann syndrome 2016-06-14 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000308475 SCV000604097 benign Stüve-Wiedemann syndrome 2020-08-27 criteria provided, single submitter clinical testing
Invitae RCV001519778 SCV001728707 benign not provided 2020-11-25 criteria provided, single submitter clinical testing
Natera, Inc. RCV000308475 SCV001462559 benign Stüve-Wiedemann syndrome 2020-09-16 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.