Genetics University — Research, Education, Medical Genetics
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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.