Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		0.700 GeneticVariation LHGDN Transmembrane activator and calcium-modulating cyclophilin ligand interactor mutations in common variable immunodeficiency: clinical and immunologic outcomes in heterozygotes. 17983875

2007
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		0.700 GeneticVariation LHGDN Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency. 17392797

2007
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		0.700 GeneticVariation LHGDN Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency. 17392798

2007
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		0.700 GeneticVariation LHGDN Using a candidate gene approach, we identified homozygous and heterozygous mutations in TNFRSF13B, encoding TACI, in 13 individuals with common variable immunodeficiency. 16007087

2005