ClinVar Miner

List of variants reported as likely benign for MOGS-CDG

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 11
Download table as spreadsheet
HGVS dbSNP
NM_006302.3(MOGS):c.1245C>T (p.Ile415=) rs34838944
NM_006302.3(MOGS):c.1294G>C (p.Val432Leu) rs552488837
NM_006302.3(MOGS):c.1509A>C (p.Leu503=) rs759481390
NM_006302.3(MOGS):c.1581C>A (p.Asp527Glu) rs200508287
NM_006302.3(MOGS):c.1851T>A (p.His617Gln) rs199939051
NM_006302.3(MOGS):c.2055T>C (p.Tyr685=) rs202094225
NM_006302.3(MOGS):c.249C>G (p.Ala83=) rs764778419
NM_006302.3(MOGS):c.297C>T (p.Tyr99=) rs375679925
NM_006302.3(MOGS):c.375C>G (p.Gly125=) rs369972550
NM_006302.3(MOGS):c.499A>C (p.Arg167=) rs371747622
NM_006302.3(MOGS):c.664G>A (p.Gly222Arg) rs3213671

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.