Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

SLC26A3

solute carrier family 26 member 3

Chromosome
7
Cytoband
7q22.3-q31.1
Variants (rsID)
22

SLC26A3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q22.3-q31.1). Its official name is “solute carrier family 26 member 3”. The reference table lists 22 variants (rsID) for this gene.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Clinically classified variants

5 reference-table entries with clinical significance.

  • rs34407351Benignsingle nucleotide variantCongenital secretory diarrhea, chloride type
  • rs3735605Benignsingle nucleotide variantCongenital secretory diarrhea, chloride type
  • rs386833479Likely pathogenicsingle nucleotide variantCongenital secretory diarrhea, chloride type
  • rs386833480Likely pathogenicsingle nucleotide variantCongenital secretory diarrhea, chloride type
  • rs386833446Uncertain significancesingle nucleotide variantCongenital secretory diarrhea, chloride type

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.