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.
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
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
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
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
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
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
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
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
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 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
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
Chronic hepatitis C genotype 1
CUI: C4049392
Disease: Chronic hepatitis C genotype 1
1 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.040 1.000 4 2011 2014
HIV Coinfection
CUI: C4505456
Disease: HIV Coinfection
3 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.030 1.000 3 2013 2014
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 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
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
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
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
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
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
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
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.100 0.818 11 2012 2015
Hepatitis B, Chronic
CUI: C0524909
Disease: Hepatitis B, Chronic
84 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.050 1.000 5 2012 2015