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Gene entry

SLC12A3

solute carrier family 12 member 3

Chromosome
16
Cytoband
16q13
Variants (rsID)
38

SLC12A3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q13). Its official name is “solute carrier family 12 member 3”. The reference table lists 38 variants (rsID) for this gene.

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Clinically classified variants

11 reference-table entries with clinical significance.

  • rs118121751Benignsingle nucleotide variantFamilial hypokalemia-hypomagnesemia
  • rs1529927Benignsingle nucleotide variantFamilial hypokalemia-hypomagnesemia
  • rs2304483Benignsingle nucleotide variantFamilial hypokalemia-hypomagnesemia
  • rs35797045Benignsingle nucleotide variantFamilial hypokalemia-hypomagnesemia
  • rs5801Benignsingle nucleotide variantFamilial hypokalemia-hypomagnesemia
  • rs139329616Conflicting interpretationssingle nucleotide variantFamilial hypokalemia-hypomagnesemia
  • rs200253241Conflicting interpretationssingle nucleotide variantFamilial hypokalemia-hypomagnesemia
  • rs121909382Pathogenicsingle nucleotide variantFamilial hypokalemia-hypomagnesemia
  • rs140012781Pathogenicsingle nucleotide variantFamilial hypokalemia-hypomagnesemia|Familial hypokalemia-hypomagnesemia|Bartter syndrome
  • rs267607050Pathogenicsingle nucleotide variantFamilial hypokalemia-hypomagnesemia
  • rs374163823Pathogenicsingle nucleotide variantFamilial hypokalemia-hypomagnesemia

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.