Gene entry
SLC52A3
solute carrier family 52 member 3
- Chromosome
- 20
- Cytoband
- 20p13
- Variants (rsID)
- 16
SLC52A3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 20 (region 20p13). Its official name is “solute carrier family 52 member 3”. The reference table lists 16 variants (rsID) for this gene.
Clinically classified variants
11 reference-table entries with clinical significance.
- rs139486822Benignsingle nucleotide variantBrown-Vialetto-van Laere syndrome 1
- rs35655964Benignsingle nucleotide variantBrown-Vialetto-van Laere syndrome 1
- rs3746802Benignsingle nucleotide variantBrown-Vialetto-van Laere syndrome 1
- rs3746804Benignsingle nucleotide variantBrown-Vialetto-van Laere syndrome 1
- rs3746807Benignsingle nucleotide variantBrown-Vialetto-van Laere syndrome 1
- rs6054605Benignsingle nucleotide variantBrown-Vialetto-van Laere syndrome 1
- rs76947760Benignsingle nucleotide variantBrown-Vialetto-van Laere syndrome 1
- rs910857Benignsingle nucleotide variantBrown-Vialetto-van Laere syndrome 1|Progressive bulbar palsy of childhood
- rs267606686Conflicting interpretationssingle nucleotide variantBrown-Vialetto-van Laere syndrome 1|Progressive bulbar palsy of childhood
- rs267606684Uncertain significancesingle nucleotide variantBrown-Vialetto-van Laere syndrome 1
- rs370499474Uncertain significancesingle nucleotide variantBrown-Vialetto-van Laere syndrome 1
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.