Gene entry
SLC3A1
solute carrier family 3 member 1
- Chromosome
- 2
- Cytoband
- 2p21
- Variants (rsID)
- 17
SLC3A1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2p21). Its official name is “solute carrier family 3 member 1”. The reference table lists 17 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs121912691Pathogenicsingle nucleotide variantCystinuria|See cases
- rs121912696Uncertain significancesingle nucleotide variantCystinuria
- rs121912697Uncertain significancesingle nucleotide variantCystinuria
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.