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: rs12722561
rs12722561
IL2RA
1.000 0.080 10 6027930 intron variant C/A;T snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2016 2016
dbSNP: rs12722547
rs12722547
IL2RA
10 6030130 intron variant G/C snv 7.8E-03
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs4747846
rs4747846
IL2RA ; LOC107984201
10 6032488 intron variant G/A;C;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2017 2017
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: rs12722515
rs12722515
IL2RA
1.000 0.040 10 6039267 intron variant C/A snv 0.13
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 2 2012 2015
dbSNP: rs12722515
rs12722515
IL2RA
1.000 0.040 10 6039267 intron variant C/A snv 0.13
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2015 2015
dbSNP: rs1107345
rs1107345
IL2RA
0.925 0.160 10 6045332 intron variant G/T snv 0.18
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2019 2019
dbSNP: rs1107345
rs1107345
IL2RA
0.925 0.160 10 6045332 intron variant G/T snv 0.18
CUI: C1367654
Disease: Marginal Zone B-Cell Lymphoma
Marginal Zone B-Cell Lymphoma 		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: 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: rs12253981
rs12253981
IL2RA
1.000 0.080 10 6050383 intron variant T/G snv 0.29
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2017 2017
dbSNP: rs12722502
rs12722502
IL2RA
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 2 2019 2019
dbSNP: rs12722502
rs12722502
IL2RA
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma 		0.700 1.000 1 2019 2019
dbSNP: rs12722502
rs12722502
IL2RA
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs12722502
rs12722502
IL2RA
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		0.700 1.000 1 2019 2019
dbSNP: rs61839660
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 2 2016 2017
dbSNP: rs61839660
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 2 2017 2018
dbSNP: rs61839660
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.800 1.000 2 2012 2015
dbSNP: rs61839660
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016