rs2104286, IL2RA

N. diseases: 25
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.
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.900 1.000 14 2007 2019
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.830 1.000 5 2012 2015
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.700 1.000 1 2016 2016
Cholangitis, Sclerosing
CUI: C0008313
Disease: Cholangitis, Sclerosing
276 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.700 1.000 1 2016 2016
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.700 1.000 1 2016 2016
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.700 1.000 1 2016 2016
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.700 1.000 1 2016 2016
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.060 0.833 6 2009 2019
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.020 1.000 2 2009 2015
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.020 0.500 2 2009 2015
Acute anterior uveitis
CUI: C0701807
Disease: Acute anterior uveitis
30 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.010 1.000 1 2011 2011
Addison's disease due to autoimmunity
CUI: C0271737
Disease: Addison's disease due to autoimmunity
18 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.010 1.000 1 2015 2015
Autoimmune Primary Adrenal Insufficiency
CUI: C2103602
Disease: Autoimmune Primary Adrenal Insufficiency
18 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.010 1.000 1 2015 2015
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.010 1.000 1 2014 2014
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.010 1 2010 2010
Irritable Bowel Syndrome
CUI: C0022104
Disease: Irritable Bowel Syndrome
52 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.010 1.000 1 2014 2014
Juvenile arthritis
CUI: C3495559
Disease: Juvenile arthritis
128 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.010 1.000 1 2009 2009
Lupus Erythematosus
CUI: C0409974
Disease: Lupus Erythematosus
44 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.010 1.000 1 2015 2015
Lupus Erythematosus, Discoid
CUI: C0024138
Disease: Lupus Erythematosus, Discoid
46 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.010 1.000 1 2015 2015
Lupus Vulgaris
CUI: C0024131
Disease: Lupus Vulgaris
44 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.010 1.000 1 2015 2015
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.010 1.000 1 2014 2014
Superficial ulcer
CUI: C0333307
Disease: Superficial ulcer
10 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.010 1.000 1 2014 2014
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.010 1 2012 2012
Uveitis
CUI: C0042164
Disease: Uveitis
43 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.010 1.000 1 2011 2011
Uveitis, Intermediate
CUI: C0042166
Disease: Uveitis, Intermediate
10 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.010 1.000 1 2011 2011