Gene entry
SLC52A2
solute carrier family 52 member 2
- Chromosome
- 8
- Cytoband
- 8q24.3
- Variants (rsID)
- 7
SLC52A2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 8 (region 8q24.3). Its official name is “solute carrier family 52 member 2”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs34383175Benignsingle nucleotide variant
- rs368924997Conflicting interpretationssingle nucleotide variantBrown-Vialetto-van Laere syndrome 2
- rs148234606Pathogenicsingle nucleotide variantBrown-Vialetto-van Laere syndrome 2|Inborn genetic diseases
- rs375088539Pathogenicsingle nucleotide variantBrown-Vialetto-van Laere syndrome 2|Brown-Vialetto-van Laere syndrome 1
- rs397514657Pathogenicsingle nucleotide variantBrown-Vialetto-van Laere syndrome 2
- rs754320812Pathogenicsingle nucleotide variantBrown-Vialetto-van Laere syndrome 2|Inborn genetic diseases
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.