Gene entry
ALG12
ALG12 alpha-1,6-mannosyltransferase
- Chromosome
- 22
- Cytoband
- 22q13.33
- Variants (rsID)
- 7
ALG12 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 22 (region 22q13.33). Its official name is “ALG12 alpha-1,6-mannosyltransferase”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs3922872Benignsingle nucleotide variantALG12-congenital disorder of glycosylation
- rs62233155Benignsingle nucleotide variantALG12-congenital disorder of glycosylation
- rs78916708Benignsingle nucleotide variantALG12-congenital disorder of glycosylation
- rs121907932Conflicting interpretationssingle nucleotide variantALG12-congenital disorder of glycosylation
- rs121907933Likely pathogenicsingle nucleotide variantALG12-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.