Gene entry
SLC5A1
solute carrier family 5 member 1
- Chromosome
- 22
- Cytoband
- 22q12.3
- Variants (rsID)
- 13
SLC5A1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 22 (region 22q12.3). Its official name is “solute carrier family 5 member 1”. The reference table lists 13 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs17683807Benignsingle nucleotide variantCongenital glucose-galactose malabsorption
- rs121912669Uncertain significancesingle nucleotide variantCongenital glucose-galactose malabsorption
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.
