rs1555908409, RAC2

N. diseases: 7
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Abnormality of cellular immune system
CUI: C4023612
Disease: Abnormality of cellular immune system
3 0.851 0.160 22 37232842 missense variant C/T snv 0.700 0
Abnormality of T cell physiology
CUI: C4023166
Disease: Abnormality of T cell physiology
3 0.851 0.160 22 37232842 missense variant C/T snv 0.700 0
Combined immunodeficiency
CUI: C0494261
Disease: Combined immunodeficiency
11 0.851 0.160 22 37232842 missense variant C/T snv 0.700 0
Immunologic Deficiency Syndromes
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
31 0.851 0.160 22 37232842 missense variant C/T snv 0.700 0
Lymphopenia
CUI: C0024312
Disease: Lymphopenia
16 0.851 0.160 22 37232842 missense variant C/T snv 0.700 0
Neutrophil Immunodeficiency Syndrome
CUI: C1842398
Disease: Neutrophil Immunodeficiency Syndrome
2 0.851 0.160 22 37232842 missense variant C/T snv 0.700 0
Severe Combined Immunodeficiency
CUI: C0085110
Disease: Severe Combined Immunodeficiency
46 0.851 0.160 22 37232842 missense variant C/T snv 0.700 0