Gene entry
STT3A
STT3 oligosaccharyltransferase complex catalytic subunit A
- Chromosome
- 11
- Cytoband
- 11q24.2
- Variants (rsID)
- 13
STT3A is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q24.2). Its official name is “STT3 oligosaccharyltransferase complex catalytic subunit A”. The reference table lists 13 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs2241501Benignsingle nucleotide variantSTT3A-congenital disorder of glycosylation
- rs2241502Benignsingle nucleotide variantSTT3A-congenital disorder of glycosylation
- rs34079079Benignsingle nucleotide variant
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.