rs2069812, IL5

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.
B-Cell Lymphomas
CUI: C0079731
Disease: B-Cell Lymphomas
42 0.851 0.240 5 132544224 intron variant A/G snv 0.54 0.010 1.000 1 2011 2011
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.851 0.240 5 132544224 intron variant A/G snv 0.54 0.010 1.000 1 2010 2010
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.851 0.240 5 132544224 intron variant A/G snv 0.54 0.010 1.000 1 2011 2011
T-Cell Lymphoma
CUI: C0079772
Disease: T-Cell Lymphoma
24 0.851 0.240 5 132544224 intron variant A/G snv 0.54 0.010 1.000 1 2011 2011
Thyroid associated opthalmopathies
CUI: C0339143
Disease: Thyroid associated opthalmopathies
49 0.851 0.240 5 132544224 intron variant A/G snv 0.54 0.010 1.000 1 2010 2010