Gene entry
MOGS
mannosyl-oligosaccharide glucosidase
- Chromosome
- 2
- Cytoband
- 2p13.1
- Variants (rsID)
- 8
MOGS is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2p13.1). Its official name is “mannosyl-oligosaccharide glucosidase”. The reference table lists 8 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs13405869Benignsingle nucleotide variantMOGS-congenital disorder of glycosylation
- rs142032474Benignsingle nucleotide variantMOGS-congenital disorder of glycosylation
- rs184209905Benignsingle nucleotide variantMOGS-congenital disorder of glycosylation
- rs369653963Benignsingle nucleotide variantMOGS-congenital disorder of glycosylation
- rs202094225Conflicting interpretationssingle nucleotide variantMOGS-congenital disorder of glycosylation
- rs587777323Pathogenicsingle nucleotide variantMOGS-congenital disorder of glycosylation
- rs186098891Uncertain significancesingle nucleotide variantMOGS-congenital disorder of glycosylation
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.