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.
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