Gene entry
SLC6A1
solute carrier family 6 member 1
- Chromosome
- 3
- Cytoband
- 3p25.3
- Variants (rsID)
- 28
SLC6A1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p25.3). Its official name is “solute carrier family 6 member 1”. The reference table lists 28 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs191293931Conflicting interpretationssingle nucleotide variantMyoclonic-atonic epilepsy|History of neurodevelopmental disorder
- rs794726860Pathogenicsingle nucleotide variantMyoclonic-atonic epilepsy|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.