Disease: IMMUNODEFICIENCY, COMMON VARIABLE, 2 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs72553882
rs72553882
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C3150354
Disease:
IMMUNODEFICIENCY, COMMON VARIABLE, 2 		C 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