Gene entry
TNFRSF13C
TNF receptor superfamily member 13C
- Chromosome
- 22
- Cytoband
- 22q13.2
- Variants (rsID)
- 1
TNFRSF13C is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 22 (region 22q13.2). Its official name is “TNF receptor superfamily member 13C”. The reference table lists 1 variant (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs61756766Conflicting interpretationssingle nucleotide variantImmunodeficiency, common variable, 4
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
