ClinVar Miner

List of variants reported as benign for Isovaleryl-CoA dehydrogenase deficiency

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
Download table as spreadsheet
NM_002225.5(IVD):c.*1471G>A rs4923865
NM_002225.5(IVD):c.*1577C>G rs11630850
NM_002225.5(IVD):c.*1610C>T rs11630878
NM_002225.5(IVD):c.*1893del rs398026948
NM_002225.5(IVD):c.*2275T>C rs11790
NM_002225.5(IVD):c.*261G>A rs2075624
NM_002225.5(IVD):c.*2844T>C rs7207
NM_002225.5(IVD):c.*3036del rs5812161
NM_002225.5(IVD):c.*808C>G rs2075625
NM_002225.5(IVD):c.234+14T>C rs2289331

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.