Genetics University — Research, Education, Medical Genetics
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Gene entry

SLC6A4

solute carrier family 6 member 4

Chromosome
17
Cytoband
17q11.2
Variants (rsID)
13

SLC6A4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q11.2). Its official name is “solute carrier family 6 member 4”. The reference table lists 13 variants (rsID) for this gene.

Clinically classified variants

3 reference-table entries with clinical significance.

  • rs1042173Likely benignsingle nucleotide variantBehavior disorder
  • rs3813034Likely benignsingle nucleotide variantBehavior disorder
  • rs7224199Likely benignsingle nucleotide variantBehavior disorder

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.