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.
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, 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
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
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 hypoplasia of adrenal gland
CUI: C0220766
Disease: Congenital hypoplasia of adrenal gland
13 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.030 1.000 3 2011 2017
Chronic liver disease
CUI: C0341439
Disease: Chronic liver disease
14 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.020 1.000 2 2014 2015
Icterus
CUI: C0022346
Disease: Icterus
17 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.020 1.000 2 2012 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
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
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
Cytomegalovirus Infections
CUI: C0010823
Disease: Cytomegalovirus Infections
26 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.040 0.750 4 2014 2019
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
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
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
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
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
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
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
Fatty Liver
CUI: C0015695
Disease: Fatty Liver
35 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.020 1.000 2 2012 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
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
Hepatitis
CUI: C0019158
Disease: Hepatitis
42 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.040 0.750 4 2011 2017
Virus Diseases
CUI: C0042769
Disease: Virus Diseases
42 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.020 1.000 2 2010 2017