rs907715, IL21

N. diseases: 11
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.
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.752 0.520 4 122613898 intron variant C/T snv 0.35 0.030 1.000 3 2008 2015
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.752 0.520 4 122613898 intron variant C/T snv 0.35 0.020 1.000 2 2011 2018
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.752 0.520 4 122613898 intron variant C/T snv 0.35 0.010 1.000 1 2015 2015
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.752 0.520 4 122613898 intron variant C/T snv 0.35 0.010 1.000 1 2018 2018
Cryptorchidism
CUI: C0010417
Disease: Cryptorchidism
80 0.752 0.520 4 122613898 intron variant C/T snv 0.35 0.010 1.000 1 2016 2016
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.752 0.520 4 122613898 intron variant C/T snv 0.35 0.010 1 2010 2010
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.752 0.520 4 122613898 intron variant C/T snv 0.35 0.010 1.000 1 2014 2014
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.752 0.520 4 122613898 intron variant C/T snv 0.35 0.010 1.000 1 2016 2016
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.752 0.520 4 122613898 intron variant C/T snv 0.35 0.010 1 2010 2010
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.752 0.520 4 122613898 intron variant C/T snv 0.35 0.010 1.000 1 2013 2013
Thyroid associated opthalmopathies
CUI: C0339143
Disease: Thyroid associated opthalmopathies
49 0.752 0.520 4 122613898 intron variant C/T snv 0.35 0.010 1.000 1 2011 2011