ClinVar Miner

List of variants studied for congenital disorder of glycosylation type I by Institute of Human Genetics,Klinikum rechts der Isar

Included ClinVar conditions (31):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
Download table as spreadsheet
NM_004341.5(CAD):c.1843-3C>T rs1057519262
NM_004341.5(CAD):c.5365C>T (p.Arg1789Ter) rs62130681
NM_004341.5(CAD):c.98T>G (p.Met33Arg) rs751610198
NM_004870.4(MPDU1):c.218G>A (p.Gly73Glu) rs104894586

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.