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.
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
Cholangiocarcinoma
CUI: C0206698
Disease: Cholangiocarcinoma
43 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.020 1.000 2 2013 2016
Chronic hepatitis C virus genotype 1
CUI: C3805156
Disease: Chronic hepatitis C virus genotype 1
2 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.020 1.000 2 2012 2014
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
Chronic viral hepatitis
CUI: C0276623
Disease: Chronic viral hepatitis
8 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.020 1.000 2 2011 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
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
HIV Infections
CUI: C0019693
Disease: HIV Infections
142 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.020 0.500 2 2010 2018
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
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
Tropical Spastic Paraparesis
CUI: C0030481
Disease: Tropical Spastic Paraparesis
4 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.020 1.000 2 2012 2015
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
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