rs706778, IL2RA

N. diseases: 19
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.
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.810 0.750 4 2011 2019
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.800 1.000 3 2010 2019
Diabetes Mellitus, Insulin-Dependent
954 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.750 1.000 6 2007 2015
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
142 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.700 1.000 2 2015 2019
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
132 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.700 1.000 2 2015 2019
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
141 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.700 1.000 2 2015 2019
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.700 1.000 1 2015 2015
Autoimmune thyroiditis
CUI: C0920350
Disease: Autoimmune thyroiditis
76 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.700 1.000 1 2015 2015
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.700 1.000 1 2015 2015
Common Variable Immunodeficiency
CUI: C0009447
Disease: Common Variable Immunodeficiency
85 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.700 1.000 1 2015 2015
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.700 1.000 1 2015 2015
Immune System Diseases
CUI: C0021053
Disease: Immune System Diseases
116 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.700 1.000 1 2011 2011
Juvenile arthritis
CUI: C3495559
Disease: Juvenile arthritis
128 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.700 1.000 1 2015 2015
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.700 1.000 1 2015 2015
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.700 1.000 1 2011 2011
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.700 1.000 1 2015 2015
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.700 1.000 1 2015 2015
Autoimmune thyroid disease (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
54 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.010 1.000 1 2010 2010
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.010 1.000 1 2010 2010