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Gene entry

SLC22A12

solute carrier family 22 member 12

Chromosome
11
Cytoband
11q13.1
Variants (rsID)
18

SLC22A12 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q13.1). Its official name is “solute carrier family 22 member 12”. The reference table lists 18 variants (rsID) for this gene.

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Clinically classified variants

6 reference-table entries with clinical significance.

  • rs11231825Benignsingle nucleotide variantDalmatian hypouricemia
  • rs1630320Benignsingle nucleotide variantDalmatian hypouricemia
  • rs3825017Benignsingle nucleotide variantDalmatian hypouricemia
  • rs7932775Benignsingle nucleotide variantDalmatian hypouricemia
  • rs9734313Benignsingle nucleotide variantDalmatian hypouricemia
  • rs121907892Pathogenicsingle nucleotide variantDalmatian hypouricemia

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.