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Gene entry

SLC6A5

solute carrier family 6 member 5

Chromosome
11
Cytoband
11p15.1
Variants (rsID)
30

SLC6A5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11p15.1). Its official name is “solute carrier family 6 member 5”. The reference table lists 30 variants (rsID) for this gene.

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Clinically classified variants

7 reference-table entries with clinical significance.

  • rs16906628Benignsingle nucleotide variantHyperekplexia|Hyperekplexia 3
  • rs1805091Benignsingle nucleotide variantHyperekplexia|Hyperekplexia 3
  • rs2276433Benignsingle nucleotide variantHyperekplexia|Hyperekplexia 3
  • rs61736602Benignsingle nucleotide variantHyperekplexia|Hyperekplexia 3
  • rs75450512Likely benignsingle nucleotide variantHyperekplexia|Hyperekplexia 3
  • rs121908494Pathogenicsingle nucleotide variantHyperekplexia 3
  • rs121908498Uncertain significancesingle nucleotide variantHyperekplexia 3

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.