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Gene entry

SLC10A1

solute carrier family 10 member 1

Chromosome
14
Cytoband
14q24.1
Variants (rsID)
18

SLC10A1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q24.1). Its official name is “solute carrier family 10 member 1”. The reference table lists 18 variants (rsID) for this gene.

Clinically classified variants

3 reference-table entries with clinical significance.

  • rs2296651Benignsingle nucleotide variantHypercholanemia, familial, 2|Hepatitis B virus, resistance to
  • rs189313778Uncertain significancesingle nucleotide variant
  • rs200282964Uncertain significancesingle nucleotide variant

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.