Gene entry
ALG6
ALG6 alpha-1,3-glucosyltransferase
- Chromosome
- 1
- Cytoband
- 1p31.3
- Variants (rsID)
- 17
ALG6 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p31.3). Its official name is “ALG6 alpha-1,3-glucosyltransferase”. The reference table lists 17 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs116660078Benignsingle nucleotide variantALG6-congenital disorder of glycosylation 1C
- rs35383149Benignsingle nucleotide variantALG6-congenital disorder of glycosylation 1C
- rs4630153Benignsingle nucleotide variantALG6-congenital disorder of glycosylation 1C
- rs183861757Conflicting interpretationssingle nucleotide variantALG6-congenital disorder of glycosylation 1C
- rs121908443Pathogenicsingle nucleotide variantALG6-congenital disorder of glycosylation 1C
- rs199682486Pathogenicsingle nucleotide variantALG6-congenital disorder of glycosylation 1C
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.