Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs9663421
rs9663421
IL2RA
1.000 0.080 10 6013641 intron variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs7909519
rs7909519
IL2RA
0.807 0.120 10 6047878 intron variant T/G snv 7.2E-02
CUI: C3898105
Disease: Oligoarticular Juvenile Idiopathic Arthritis
Oligoarticular Juvenile Idiopathic Arthritis 		0.800 1.000 1 2013 2013
dbSNP: rs7909519
rs7909519
IL2RA
0.807 0.120 10 6047878 intron variant T/G snv 7.2E-02
CUI: C3890205
Disease: Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative 		0.700 1.000 1 2013 2013
dbSNP: rs7909519
rs7909519
IL2RA
0.807 0.120 10 6047878 intron variant T/G snv 7.2E-02
CUI: C1858558
Disease: Rheumatoid Arthritis, Systemic Juvenile
Rheumatoid Arthritis, Systemic Juvenile 		0.700 1.000 1 2013 2013
dbSNP: rs7909519
rs7909519
IL2RA
0.807 0.120 10 6047878 intron variant T/G snv 7.2E-02
CUI: C2931171
Disease: Juvenile pauciarticular chronic arthritis
Juvenile pauciarticular chronic arthritis 		0.700 1.000 1 2013 2013
dbSNP: rs7909519
rs7909519
IL2RA
0.807 0.120 10 6047878 intron variant T/G snv 7.2E-02
CUI: C0087031
Disease: Juvenile-Onset Still Disease
Juvenile-Onset Still Disease 		0.700 1.000 1 2013 2013
dbSNP: rs7909519
rs7909519
IL2RA
0.807 0.120 10 6047878 intron variant T/G snv 7.2E-02
CUI: C1384600
Disease: Systemic onset juvenile chronic arthritis
Systemic onset juvenile chronic arthritis 		0.700 1.000 1 2013 2013
dbSNP: rs7893467
rs7893467
IL2RA
1.000 0.040 10 6037072 intron variant G/C;T snv
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2019 2019
dbSNP: rs7090504
rs7090504
IL2RA
10 6049054 intron variant T/A snv 0.16
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs706779
rs706779
IL2RA
0.827 0.160 10 6056861 intron variant T/C snv 0.48
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.810 1.000 2 2010 2016
dbSNP: rs706779
rs706779
IL2RA
0.827 0.160 10 6056861 intron variant T/C snv 0.48
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2012 2012
dbSNP: rs706779
rs706779
IL2RA
0.827 0.160 10 6056861 intron variant T/C snv 0.48
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		0.700 1.000 1 2012 2012
dbSNP: rs706779
rs706779
IL2RA
0.827 0.160 10 6056861 intron variant T/C snv 0.48
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		0.700 1.000 1 2012 2012
dbSNP: rs706778
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 3 2010 2019
dbSNP: rs706778
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.810 0.750 2 2011 2019
dbSNP: rs706778
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 2 2015 2019
dbSNP: rs706778
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 2 2015 2019
dbSNP: rs706778
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 2 2015 2019
dbSNP: rs706778
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		0.700 1.000 1 2015 2015
dbSNP: rs706778
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2015 2015
dbSNP: rs706778
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		0.700 1.000 1 2015 2015
dbSNP: rs706778
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2015 2015
dbSNP: rs706778
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2015 2015
dbSNP: rs706778
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2015 2015
dbSNP: rs706778
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.750 1.000 1 2007 2015