Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs72553875
rs72553875
TNFRSF13B
GT 0.700 CausalMutation CLINVAR Clinical Associations of Biallelic and Monoallelic TNFRSF13B Variants in Italian Primary Antibody Deficiency Syndromes. 27123465

2016
dbSNP: rs72553875
rs72553875
TNFRSF13B
GT 0.700 CausalMutation CLINVAR TNF receptor superfamily member 13b (TNFRSF13B) hemizygosity reveals transmembrane activator and CAML interactor haploinsufficiency at later stages of B-cell development. 26100089

2015
dbSNP: rs72553875
rs72553875
TNFRSF13B
GT 0.700 CausalMutation CLINVAR Individualized iterative phenotyping for genome-wide analysis of loss-of-function mutations. 26046366

2015
dbSNP: rs72553875
rs72553875
TNFRSF13B
GT 0.700 CausalMutation CLINVAR Sequence variants of the TNFRSF13B gene in Czech CVID and IgAD patients in the context of other populations. 22884984

2012
dbSNP: rs72553875
rs72553875
TNFRSF13B
GT 0.700 CausalMutation CLINVAR Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes. 18981294

2009
dbSNP: rs72553875
rs72553875
TNFRSF13B
GT 0.700 CausalMutation CLINVAR Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency. 17392798

2007
dbSNP: rs72553875
rs72553875
TNFRSF13B
GT 0.700 CausalMutation CLINVAR TACI is mutant in common variable immunodeficiency and IgA deficiency. 16007086

2005
dbSNP: rs72553875
rs72553875
TNFRSF13B
GT 0.700 GeneticVariation CLINVAR