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Gene entry

SLC6A3

solute carrier family 6 member 3

Chromosome
5
Cytoband
5p15.33
Variants (rsID)
31

SLC6A3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5p15.33). Its official name is “solute carrier family 6 member 3”. The reference table lists 31 variants (rsID) for this gene.

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Clinically classified variants

4 reference-table entries with clinical significance.

  • rs460000Benignsingle nucleotide variantParkinsonism-dystonia, infantile, 1|Parkinsonism-dystonia, infantile
  • rs6347Benignsingle nucleotide variantParkinsonism-dystonia, infantile, 1|Parkinsonism-dystonia, infantile
  • rs115282473Likely benignsingle nucleotide variantParkinsonism-dystonia, infantile
  • rs577802449Uncertain significancesingle nucleotide variantParkinsonism-dystonia, infantile, 1|Parkinsonism-dystonia, infantile

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.