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.
Infectious Mononucleosis
CUI: C0021345
Disease: Infectious Mononucleosis
4 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2014 2014
Post-transplant lymphoproliferative disorder
CUI: C0432487
Disease: Post-transplant lymphoproliferative disorder
2 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2014 2014
Recurrent hepatitis
CUI: C3887641
Disease: Recurrent hepatitis
5 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2014 2014
Compensated cirrhosis
CUI: C1608426
Disease: Compensated cirrhosis
2 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.020 1.000 2 2015 2016
Mixed cryoglobulinemia
CUI: C0543697
Disease: Mixed cryoglobulinemia
5 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.020 1.000 2 2015 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
HTLV-I Infections
CUI: C0020097
Disease: HTLV-I Infections
5 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2015 2015
Lower Urinary Tract Symptoms
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
30 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2015 2015
Occult chronic type B viral hepatitis
CUI: C4075603
Disease: Occult chronic type B viral hepatitis
4 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2015 2015
Hepatitis, Chronic
CUI: C0019189
Disease: Hepatitis, Chronic
10 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.030 1.000 3 2016 2018
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
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
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
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
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 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
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
Hepatocarcinogenesis
CUI: C1512409
Disease: Hepatocarcinogenesis
24 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1 2017 2017
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
140 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2017 2017
Thalassemia
CUI: C0039730
Disease: Thalassemia
18 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2017 2017