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.
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2012 2012
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: 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
Asthma
CUI: C0004096
Disease: Asthma
1536 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1 2017 2017
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
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2018 2018
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2018 2018
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
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
Hemophilia A
CUI: C0019069
Disease: Hemophilia A
295 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2013 2013
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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