rs8099917, None

N. diseases: 60
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 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.100 0.965 113 2010 2019
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
80 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.900 1.000 18 2009 2019
Pseudohyperkalemia Cardiff
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
60 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.100 0.933 15 2011 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.090 0.889 9 2012 2019
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.080 0.750 8 2011 2017
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
64 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.070 1.000 7 2010 2019
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.060 1.000 6 2011 2017
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.040 1.000 4 2013 2019
Fatty Liver
CUI: C0015695
Disease: Fatty Liver
35 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.030 1.000 3 2013 2017
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.030 0.667 3 2012 2017
Mixed cryoglobulinemia
CUI: C0543697
Disease: Mixed cryoglobulinemia
5 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.030 1.000 3 2013 2017
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
75 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.030 1.000 3 2013 2017
Bronchiolitis
CUI: C0006271
Disease: Bronchiolitis
32 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.020 1.000 2 2012 2020
Chronic hepatitis C virus genotype 1
2 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.020 1.000 2 2012 2014
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.020 1.000 2 2014 2017
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.020 1.000 2 2012 2016
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.020 1.000 2 2017 2018
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
115 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.020 1.000 2 2017 2018
Icterus
CUI: C0022346
Disease: Icterus
17 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.020 1.000 2 2010 2019
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.020 0.500 2 2012 2012
Recurrent hepatitis
CUI: C3887641
Disease: Recurrent hepatitis
5 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.020 1.000 2 2012 2014
Acute hepatitis C
CUI: C0400914
Disease: Acute hepatitis C
2 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2012 2012
Acute infectious disease
CUI: C0275518
Disease: Acute infectious disease
5 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2017 2017
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
176 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1 2017 2017
Anemia
CUI: C0002871
Disease: Anemia
94 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2012 2012