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.
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
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
Hepatitis Virus-Related Hepatocellular Carcinoma
2 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2013 2013
Hepatocarcinogenesis
CUI: C1512409
Disease: Hepatocarcinogenesis
24 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1 2017 2017
HIV disease progression
CUI: C1141957
Disease: HIV disease progression
5 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1 2010 2010
HIV-1 infection
CUI: C2363741
Disease: HIV-1 infection
94 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2018 2018
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
Human papilloma virus infection
CUI: C0343641
Disease: Human papilloma virus infection
42 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2019 2019
Hyperbilirubinemia
CUI: C0020433
Disease: Hyperbilirubinemia
27 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2019 2019
Hyperuricemia
CUI: C0740394
Disease: Hyperuricemia
76 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2012 2012
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
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
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
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2011 2011
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2012 2012