Gene entry
SLC52A1
solute carrier family 52 member 1
- Chromosome
- 17
- Cytoband
- 17p13.2
- Variants (rsID)
- 4
SLC52A1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17p13.2). Its official name is “solute carrier family 52 member 1”. The reference table lists 4 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs346822Benignsingle nucleotide variantAriboflavinosis
- rs139373407Uncertain significancesingle nucleotide variantAriboflavinosis
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.
