Gene entry
ST3GAL3
ST3 beta-galactoside alpha-2,3-sialyltransferase 3
- Chromosome
- 1
- Cytoband
- 1p34.1
- Variants (rsID)
- 27
ST3GAL3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p34.1). Its official name is “ST3 beta-galactoside alpha-2,3-sialyltransferase 3”. The reference table lists 27 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs37458Benignsingle nucleotide variant
- rs147330005Conflicting interpretationssingle nucleotide variantEarly infantile epileptic encephalopathy with suppression bursts
- rs201834329Uncertain significancesingle nucleotide variantEarly infantile epileptic encephalopathy with suppression bursts|History of neurodevelopmental disorder|Intellectual disability, autosomal recessive 12|Developmental and epileptic encephalopathy, 15
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.