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Gene entry

SLC6A20

solute carrier family 6 member 20

Chromosome
3
Cytoband
3p21.31
Variants (rsID)
22

SLC6A20 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p21.31). Its official name is “solute carrier family 6 member 20”. The reference table lists 22 variants (rsID) for this gene.

Clinically classified variants

2 reference-table entries with clinical significance.

  • rs17279437Benignsingle nucleotide variantHyperglycinuria|Iminoglycinuria, digenic
  • rs758386Benignsingle nucleotide variantHyperglycinuria

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.