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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.