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Gene entry

SLC12A6

solute carrier family 12 member 6

Chromosome
15
Cytoband
15q14
Variants (rsID)
24

SLC12A6 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q14). Its official name is “solute carrier family 12 member 6”. The reference table lists 24 variants (rsID) for this gene.

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Clinically classified variants

10 reference-table entries with clinical significance.

  • rs117846663Benignsingle nucleotide variantAgenesis of the corpus callosum with peripheral neuropathy
  • rs140916001Benignsingle nucleotide variantAgenesis of the corpus callosum with peripheral neuropathy
  • rs186141509Benignsingle nucleotide variantAgenesis of the corpus callosum with peripheral neuropathy
  • rs34098566Benignsingle nucleotide variantAgenesis of the corpus callosum with peripheral neuropathy
  • rs35583475Benignsingle nucleotide variantAgenesis of the corpus callosum with peripheral neuropathy
  • rs79436830Benignsingle nucleotide variantAgenesis of the corpus callosum with peripheral neuropathy
  • rs75235010Conflicting interpretationssingle nucleotide variantAgenesis of the corpus callosum with peripheral neuropathy
  • rs77122016Conflicting interpretationssingle nucleotide variantAgenesis of the corpus callosum with peripheral neuropathy
  • rs121908429Likely pathogenicsingle nucleotide variantAgenesis of the corpus callosum with peripheral neuropathy|Charcot-Marie-Tooth disease
  • rs121908427Pathogenicsingle nucleotide variantAgenesis of the corpus callosum with peripheral neuropathy|See cases

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.