rs1555908409, RAC2

N. diseases: 7
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Neutrophil Immunodeficiency Syndrome
CUI: C1842398
Disease: Neutrophil Immunodeficiency Syndrome
0.700 CausalMutation CLINVAR
Abnormality of T cell physiology
CUI: C4023166
Disease: Abnormality of T cell physiology
0.700 GeneticVariation CLINVAR
Immunologic Deficiency Syndromes
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
0.700 GeneticVariation CLINVAR
Lymphopenia
CUI: C0024312
Disease: Lymphopenia
0.700 GeneticVariation CLINVAR
Abnormality of cellular immune system
CUI: C4023612
Disease: Abnormality of cellular immune system
0.700 GeneticVariation CLINVAR
Combined immunodeficiency
CUI: C0494261
Disease: Combined immunodeficiency
0.700 GeneticVariation CLINVAR
Severe Combined Immunodeficiency
CUI: C0085110
Disease: Severe Combined Immunodeficiency
0.700 GeneticVariation CLINVAR