Gene entry
SLC10A2
solute carrier family 10 member 2
- Chromosome
- 13
- Cytoband
- 13q33.1
- Variants (rsID)
- 34
SLC10A2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 13 (region 13q33.1). Its official name is “solute carrier family 10 member 2”. The reference table lists 34 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs188096Benignsingle nucleotide variant
- rs55971546Benignsingle nucleotide variant
- rs112657170Conflicting interpretationssingle nucleotide variant
- rs56398830Conflicting interpretationssingle nucleotide variant
- rs121917848Othersingle nucleotide variantBile Acid Malabsorption, Primary, 1
- rs117447044Uncertain significancesingle nucleotide variant
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.