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.
Lower Urinary Tract Symptoms
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
30 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2015 2015
Blood Coagulation Disorders
CUI: C0005779
Disease: Blood Coagulation Disorders
31 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2017 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
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
Virus Diseases
CUI: C0042769
Disease: Virus Diseases
42 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2013 2013
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
43 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2018 2018
Iron Overload
CUI: C0282193
Disease: Iron Overload
53 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2017 2017
Human immunodeficiency virus (HIV) II infection category B1
CUI: C3854222
Disease: Human immunodeficiency virus (HIV) II infection category B1
56 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2013 2013
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
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
X-linked Adrenal Hypoplasia
CUI: C0342482
Disease: X-linked Adrenal Hypoplasia
70 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2012 2012
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
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
Hepatitis B, Chronic
CUI: C0524909
Disease: Hepatitis B, Chronic
84 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2015 2015
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
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
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
99 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2017 2017
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
beta Thalassemia
CUI: C0005283
Disease: beta Thalassemia
103 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2017 2017
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
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
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2016 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
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
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