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Gene entry

SP110

SP110 nuclear body protein

Chromosome
2
Cytoband
2q37.1
Variants (rsID)
24

SP110 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q37.1). Its official name is “SP110 nuclear body protein”. The reference table lists 24 variants (rsID) for this gene.

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Clinically classified variants

5 reference-table entries with clinical significance.

  • rs1365776Benignsingle nucleotide variantHepatic veno-occlusive disease-immunodeficiency syndrome
  • rs149485401Benignsingle nucleotide variantHepatic veno-occlusive disease-immunodeficiency syndrome
  • rs3948464Benignsingle nucleotide variantMycobacterium tuberculosis, susceptibility to|Hepatic veno-occlusive disease-immunodeficiency syndrome
  • rs41309088Benignsingle nucleotide variantHepatic veno-occlusive disease-immunodeficiency syndrome
  • rs199845488Likely pathogenicsingle nucleotide variantHepatic veno-occlusive disease-immunodeficiency syndrome

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.