ClinVar Miner

Submissions for variant NM_001127671.2(LIFR):c.143-37GT[11]

dbSNP: 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 Laboratory Services, Illumina RCV000273147 SCV000457604 uncertain significance Stuve-Wiedemann syndrome 2016-06-14 criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000727652 SCV000854956 benign not specified 2018-04-05 criteria provided, single submitter clinical testing
Invitae RCV000908352 SCV001053108 likely benign not provided 2023-11-01 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003761933 SCV001159605 benign Stüve-Wiedemann syndrome 1 2023-09-28 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.