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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.