Gene entry
TNFRSF11A
TNF receptor superfamily member 11a
- Chromosome
- 18
- Cytoband
- 18q21.33
- Variants (rsID)
- 45
TNFRSF11A is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 18 (region 18q21.33). Its official name is “TNF receptor superfamily member 11a”. The reference table lists 45 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs1805034Benignsingle nucleotide variantOsteopetrosis|Bone Paget disease|Increased bone mineral density
- rs6567272Benignsingle nucleotide variant
- rs148185533Conflicting interpretationssingle nucleotide variantBone Paget disease|Osteopetrosis|Autosomal recessive osteopetrosis 7|Familial expansile osteolysis|Paget disease of bone 2, early-onset
Other listed variants
- rs884205
- rs3826619
- rs3826620
- rs4263037
- rs4369774
- rs4940552
- rs4941129
- rs4941131
- rs6567270
- rs6567276
- rs7231887
- rs7236029
- rs7237982
- rs7239261
- rs7239667
- rs8083511
- rs8087597
- rs9646629
- rs9951012
- rs9956850
- rs11664594
- rs11877530
- rs12455775
- rs12457042
- rs12458117
- rs12954567
- rs12956925
- rs12969154
- rs12970081
- rs17069840
- rs17069895
- rs17720953
- rs34950264
- rs58112300
- rs62100865
- rs73963407
- rs75117550
- rs80277619
- rs114941408
- rs117978262
- rs144853581
- rs199921746
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.