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: rs104894650
rs104894650
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C3150354
Disease:
IMMUNODEFICIENCY, COMMON VARIABLE, 2 		T 0.700 CausalMutation CLINVAR
dbSNP: rs104894650
rs104894650
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C3150354
Disease:
IMMUNODEFICIENCY, COMMON VARIABLE, 2 		C 0.700 CausalMutation CLINVAR