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Gene entry

TNFSF11

TNF superfamily member 11

Chromosome
13
Cytoband
13q14.11
Variants (rsID)
18

TNFSF11 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 13 (region 13q14.11). Its official name is “TNF superfamily member 11”. The reference table lists 18 variants (rsID) for this gene.

Clinically classified variants

3 reference-table entries with clinical significance.

  • rs138974661Benignsingle nucleotide variantAutosomal recessive osteopetrosis 2|Increased bone mineral density
  • rs2277439Benignsingle nucleotide variantAutosomal recessive osteopetrosis 2
  • rs61761332Uncertain significancesingle nucleotide variantAutosomal recessive osteopetrosis 2

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.