ClinVar Miner

Submissions for variant NM_025207.5(FLAD1):c.526_537delinsCA (p.Ala176fs) (rs876661312)

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
Research Unit for Molecular Medicine, Department for Clinical Medicine,Aarhus University RCV000223945 SCV000266359 pathogenic Multiple acyl-CoA dehydrogenase deficiency 2016-03-14 criteria provided, single submitter research
OMIM RCV000234836 SCV000292026 pathogenic Lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency 2019-09-10 no assertion criteria provided literature only

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.