rs12979860, IFNL4

N. diseases: 84
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.
Adult T-Cell Lymphoma/Leukemia
CUI: C0023493
Disease: Adult T-Cell Lymphoma/Leukemia
11 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2012 2012
Anemia, Hemolytic
CUI: C0002878
Disease: Anemia, Hemolytic
31 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1 2017 2017
Arthropathy
CUI: C0022408
Disease: Arthropathy
10 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2016 2016
beta Thalassemia
CUI: C0005283
Disease: beta Thalassemia
103 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2017 2017
Blood Coagulation Disorders
CUI: C0005779
Disease: Blood Coagulation Disorders
31 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2017 2017
Chronic hepatitis C genotype 2
CUI: C4049395
Disease: Chronic hepatitis C genotype 2
1 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2011 2011
Chronic hepatitis C genotype 4
CUI: C4049431
Disease: Chronic hepatitis C genotype 4
3 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2014 2014
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2018 2018
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
99 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2017 2017
Coinfection
CUI: C0275524
Disease: Coinfection
11 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2016 2016
Congenital Bleeding Disorder
CUI: C3641106
Disease: Congenital Bleeding Disorder
2 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2017 2017
Cooley's anemia
CUI: C0002875
Disease: Cooley's anemia
19 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2017 2017
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2015 2015
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2015 2015
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2015 2015
Cryoglobulinemic vasculitis
CUI: C0340992
Disease: Cryoglobulinemic vasculitis
1 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2014 2014
Cytomegalovirus viremia
CUI: C0877635
Disease: Cytomegalovirus viremia
2 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2016 2016
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2016 2016
Dyspnea
CUI: C0013404
Disease: Dyspnea
26 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2018 2018
Esophageal Varices
CUI: C0014867
Disease: Esophageal Varices
5 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2013 2013
Hemophilia A
CUI: C0019069
Disease: Hemophilia A
295 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2014 2014
Hemophilia, NOS
CUI: C0684275
Disease: Hemophilia, NOS
8 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2014 2014
Hemorrhagic Fever, Crimean
CUI: C0019099
Disease: Hemorrhagic Fever, Crimean
9 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1 2019 2019
Hepatitis A
CUI: C0019159
Disease: Hepatitis A
27 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2013 2013
Hepatitis D, Chronic
CUI: C0524911
Disease: Hepatitis D, Chronic
2 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2014 2014