rs72553883, TNFRSF13B

N. diseases: 3
Source: BEFREE ×
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.
Common Variable Immunodeficiency
CUI: C0009447
Disease: Common Variable Immunodeficiency
10 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
213 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