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Gene entry

SLC4A11

solute carrier family 4 member 11

Chromosome
20
Cytoband
20p13
Variants (rsID)
13

SLC4A11 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 20 (region 20p13). Its official name is “solute carrier family 4 member 11”. The reference table lists 13 variants (rsID) for this gene.

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Clinically classified variants

7 reference-table entries with clinical significance.

  • rs34460295Benignsingle nucleotide variantCorneal dystrophy-perceptive deafness syndrome|Corneal dystrophy
  • rs58757394Benignsingle nucleotide variantCorneal dystrophy|Corneal dystrophy-perceptive deafness syndrome
  • rs121909388Likely pathogenicsingle nucleotide variantCongenital hereditary endothelial dystrophy of cornea
  • rs121909392Pathogenicsingle nucleotide variantCongenital hereditary endothelial dystrophy of cornea
  • rs121909394Pathogenicsingle nucleotide variantCorneal dystrophy-perceptive deafness syndrome
  • rs121909395Pathogenicsingle nucleotide variantCorneal dystrophy-perceptive deafness syndrome
  • rs267607066Uncertain significancesingle nucleotide variantCorneal dystrophy, Fuchs endothelial, 4

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.