rs72553883, TNFRSF13B

N. diseases: 5
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.
IMMUNODEFICIENCY, COMMON VARIABLE, 2
CUI: C3150354
Disease: IMMUNODEFICIENCY, COMMON VARIABLE, 2
9 0.851 0.080 17 16940415 missense variant G/A;T snv 2.8E-05; 5.3E-03 0.700 1.000 9 2005 2013
Immunoglobulin a deficiency 2
CUI: C1836032
Disease: Immunoglobulin a deficiency 2
3 0.851 0.080 17 16940415 missense variant G/A;T snv 2.8E-05; 5.3E-03 0.700 0
Common Variable Immunodeficiency
CUI: C0009447
Disease: Common Variable Immunodeficiency
85 0.851 0.080 17 16940415 missense variant G/A;T snv 2.8E-05; 5.3E-03 0.050 0.800 5 2005 2015
Acquired Hypogammaglobulinemia
CUI: C2936664
Disease: Acquired Hypogammaglobulinemia
4 0.851 0.080 17 16940415 missense variant G/A;T snv 2.8E-05; 5.3E-03 0.030 1.000 3 2005 2010
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.851 0.080 17 16940415 missense variant G/A;T snv 2.8E-05; 5.3E-03 0.010 1.000 1 2015 2015