Gene entry
TNFRSF13B
TNF receptor superfamily member 13B
- Chromosome
- 17
- Cytoband
- 17p11.2
- Variants (rsID)
- 23
TNFRSF13B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17p11.2). Its official name is “TNF receptor superfamily member 13B”. The reference table lists 23 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs56063729Benignsingle nucleotide variantImmunodeficiency, common variable, 2|Common Variable Immune Deficiency, Dominant
- rs74811083Benignsingle nucleotide variantCommon Variable Immune Deficiency, Dominant|Immunodeficiency, common variable, 2
- rs143027621Conflicting interpretationssingle nucleotide variantImmunodeficiency, common variable, 2
- rs34557412Conflicting interpretationssingle nucleotide variantImmunodeficiency, common variable, 2|Immunoglobulin A deficiency 2|Common Variable Immune Deficiency, Dominant|16 conditions|Severe SARS-CoV-2 infection, susceptibility to|Immunodeficiency, common variable, 1|Immunodeficiency, common variable, 2|Common variable agammaglobulinemia|Immunodeficiency, common variable, 2|Immunoglobulin A deficiency 2|Immunodeficiency, common variable, 1
- rs55916807Likely benignsingle nucleotide variantCommon Variable Immune Deficiency, Dominant|Immunodeficiency, common variable, 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.