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: rs12722486
rs12722486
IL2RA
1.000 10 6061799 intron variant C/A;T snv
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2014 2014
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: rs12722486
rs12722486
IL2RA
1.000 10 6061799 intron variant C/A;T snv
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2014 2014
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: 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: rs3118470
rs3118470
IL2RA
0.752 0.360 10 6059750 intron variant T/A;C snv
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata 		0.800 1.000 2 2010 2015
dbSNP: rs2104286
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs3118471
rs3118471
IL2RA
0.827 0.120 10 6060794 intron variant A/G snv 0.24
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs61839660
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
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: 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: rs61839660
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2018 2018
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: 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: 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: 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: 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: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		0.700 1.000 1 2015 2015
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: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2015 2015
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: rs2104286
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs3118471
rs3118471
IL2RA
0.827 0.120 10 6060794 intron variant A/G snv 0.24
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
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
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