Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

IFNGR1

interferon gamma receptor 1

Chromosome
6
Cytoband
6q23.3
Variants (rsID)
9

IFNGR1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6q23.3). Its official name is “interferon gamma receptor 1”. The reference table lists 9 variants (rsID) for this gene.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Clinically classified variants

4 reference-table entries with clinical significance.

  • rs17181471Benignsingle nucleotide variantInterferon gamma receptor deficiency|Immunodeficiency 27A|Disseminated atypical mycobacterial infection
  • rs1887415Benignsingle nucleotide variantImmunodeficiency 27A|Disseminated atypical mycobacterial infection
  • rs41288981Benignsingle nucleotide variantInterferon gamma receptor deficiency|Immunodeficiency 27A|Disseminated atypical mycobacterial infection
  • rs193922451Likely pathogenicsingle nucleotide variantInterferon gamma receptor deficiency|Disseminated atypical mycobacterial infection

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.