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TNFRSF13B

HGNC ↗

Common variable immunodeficiency and selective IgA deficiency

1 article(s) in the watch · Constitutional genetics

Curated publications

6/10

Clinical Heterogeneity of TNFRSF13B Variants: A Monogenic Cause or a Genetic Modifier?

Common variable immunodeficiency and selective IgA deficiency

Gén.18 August 2026

External references

OMIM ↗GeneReviews ↗ClinVar ↗NCBI Gene ↗

Automatic aggregation page — a clinical introduction may be added.