ClinVar Miner

List of variants reported as benign for congenital brain dysgenesis due to glutamine synthetase deficiency by Labcorp Genetics (formerly Invitae), Labcorp

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001033044.4(GLUL):c.195T>C (p.Ser65=) rs1058111 0.58837
NM_001033044.4(GLUL):c.328+19A>G rs17462824 0.07277
NM_001033044.4(GLUL):c.825G>A (p.Glu275=) rs35378126 0.01038
NM_001033044.4(GLUL):c.768C>T (p.Phe256=) rs6684136 0.00138

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.