ClinVar Miner

Submissions for variant NM_001127671.2(LIFR):c.143-37GT[15]

dbSNP: rs10637374
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 7
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000177150 SCV000228981 benign not specified 2015-01-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001522166 SCV001731650 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV001522166 SCV001949648 benign not provided 2019-08-20 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002277390 SCV002566884 likely benign Connective tissue disorder 2019-06-01 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV000177150 SCV001808856 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001522166 SCV001976312 likely benign not provided no assertion criteria provided clinical testing
Natera, Inc. RCV001832014 SCV002084278 benign Stuve-Wiedemann syndrome 2019-09-27 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.