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 C
CUI: C0019196
Disease: Hepatitis C
347 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.100 0.969 196 2009 2019
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
80 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.900 1.000 41 2009 2020
Pseudohyperkalemia Cardiff
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
60 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.100 1.000 20 2010 2017
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
64 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.100 1.000 11 2010 2019
Human immunodeficiency virus (HIV) II infection category B1
CUI: C3854222
Disease: Human immunodeficiency virus (HIV) II infection category B1
56 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.060 1.000 6 2010 2018
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
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
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
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.100 0.947 19 2011 2019
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.100 1.000 14 2011 2018
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.100 1.000 12 2011 2018
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
75 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.080 0.875 8 2011 2017
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.050 1.000 5 2011 2017
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
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
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
X-linked Adrenal Hypoplasia
CUI: C0342482
Disease: X-linked Adrenal Hypoplasia
70 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.030 1.000 3 2011 2017
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 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
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
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