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Gene entry

SLC24A1

solute carrier family 24 member 1

Chromosome
15
Cytoband
15q22.31
Variants (rsID)
11

SLC24A1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q22.31). Its official name is “solute carrier family 24 member 1”. The reference table lists 11 variants (rsID) for this gene.

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Clinically classified variants

4 reference-table entries with clinical significance.

  • rs35571449Benignsingle nucleotide variantCongenital stationary night blindness 1D
  • rs146253044Conflicting interpretationssingle nucleotide variantCongenital stationary night blindness 1D
  • rs35398714Conflicting interpretationssingle nucleotide variantCongenital stationary night blindness 1D
  • rs79327611Likely benignsingle nucleotide variantCongenital stationary night blindness 1D

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.