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Gene entry

IL2RG

interleukin 2 receptor subunit gamma

Chromosome
X
Cytoband
Xq13.1
Variants (rsID)
16

IL2RG is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq13.1). Its official name is “interleukin 2 receptor subunit gamma”. The reference table lists 16 variants (rsID) for this gene.

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Clinically classified variants

16 reference-table entries with clinical significance.

  • rs193922350Likely pathogenicsingle nucleotide variantX-linked severe combined immunodeficiency
  • rs111033617Pathogenicsingle nucleotide variantX-linked severe combined immunodeficiency
  • rs111033618Pathogenicsingle nucleotide variantCombined immunodeficiency, X-linked|Inborn genetic diseases|X-linked severe combined immunodeficiency
  • rs111033619Pathogenicsingle nucleotide variantX-linked severe combined immunodeficiency
  • rs111033620Pathogenicsingle nucleotide variantX-linked severe combined immunodeficiency
  • rs111033621Pathogenicsingle nucleotide variantX-linked severe combined immunodeficiency
  • rs111033622Pathogenicsingle nucleotide variantX-linked severe combined immunodeficiency
  • rs137852508Pathogenicsingle nucleotide variantX-linked severe combined immunodeficiency
  • rs137852509Pathogenicsingle nucleotide variantX-linked severe combined immunodeficiency
  • rs137852510Pathogenicsingle nucleotide variantCombined immunodeficiency, X-linked|X-linked severe combined immunodeficiency
  • rs193922346Pathogenicsingle nucleotide variantX-linked severe combined immunodeficiency
  • rs193922347Pathogenicsingle nucleotide variantX-linked severe combined immunodeficiency
  • rs193922348Pathogenicsingle nucleotide variantX-linked severe combined immunodeficiency
  • rs869320658Pathogenicsingle nucleotide variantX-linked severe combined immunodeficiency|Combined immunodeficiency, X-linked
  • rs869320659Pathogenicsingle nucleotide variantX-linked severe combined immunodeficiency|Combined immunodeficiency, X-linked|X-linked severe combined immunodeficiency|Combined immunodeficiency, X-linked
  • rs869320660Pathogenicsingle nucleotide variantX-linked severe combined immunodeficiency

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.