ClinVar Miner

Submissions for variant NM_001174147.2(LMX1B):c.1100G>A (p.Ser367Asn)

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
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV003993513 SCV004809457 uncertain significance Nail-patella syndrome 2024-04-04 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005040624 SCV005679888 uncertain significance Nail-patella syndrome; Nail-patella-like renal disease 2024-03-26 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.