Gene entry
SLC6A9
solute carrier family 6 member 9
- Chromosome
- 1
- Cytoband
- 1p34.1
- Variants (rsID)
- 15
SLC6A9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p34.1). Its official name is “solute carrier family 6 member 9”. The reference table lists 15 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs149105213Uncertain significancesingle nucleotide variantAtypical glycine encephalopathy
- rs201636712Uncertain significancesingle nucleotide variantAtypical glycine encephalopathy
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.
