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.
Hepatitis Virus-Related Hepatocellular Carcinoma
CUI: C1333979
Disease: 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
Obesity
CUI: C0028754
Disease: Obesity
1111 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2013 2013
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
Polycythemia Vera
CUI: C0032463
Disease: Polycythemia Vera
38 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2018 2018
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
Severe Dengue
CUI: C0019100
Disease: Severe Dengue
25 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1 2018 2018
Squamous intraepithelial lesion
CUI: C0333873
Disease: Squamous intraepithelial lesion
8 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2019 2019
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
Vitamin D Deficiency
CUI: C0042870
Disease: Vitamin D Deficiency
37 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2011 2011
Acute hepatitis C
CUI: C0400914
Disease: Acute hepatitis C
2 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.020 1.000 2 2012 2015
Anemia
CUI: C0002871
Disease: Anemia
94 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.020 1.000 2 2012 2020
Bronchiolitis
CUI: C0006271
Disease: Bronchiolitis
32 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.020 1.000 2 2012 2020