Gene entry
ALG3
ALG3 alpha-1,3- mannosyltransferase
- Chromosome
- 3
- Cytoband
- 3q27.1
- Variants (rsID)
- 12
ALG3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q27.1). Its official name is “ALG3 alpha-1,3- mannosyltransferase”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs2233463Benignsingle nucleotide variantALG3-congenital disorder of glycosylation
- rs79144888Benignsingle nucleotide variantALG3-congenital disorder of glycosylation
- rs200875721Conflicting interpretationssingle nucleotide variantALG3-congenital disorder of glycosylation
- rs763727038Conflicting interpretationssingle nucleotide variantALG3-congenital disorder of glycosylation
- rs119103236Pathogenicsingle nucleotide variantALG3-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.