ClinVar Miner

Submissions for variant NM_001370658.1(BTD):c.772C>G (p.Leu258Val)

dbSNP: rs397514388
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
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München RCV000021966 SCV001150031 pathogenic Biotinidase deficiency 2018-07-16 criteria provided, single submitter clinical testing
Baylor Genetics RCV000021966 SCV004211476 pathogenic Biotinidase deficiency 2023-03-08 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.