rs361525, TNF

N. diseases: 62
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.
Diabetes Mellitus, Insulin-Dependent
954 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.020 0.500 2 2006 2008
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.020 1.000 2 2007 2014
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.020 1.000 2 2007 2014
Exfoliation Syndrome
CUI: C0206368
Disease: Exfoliation Syndrome
74 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2009 2009
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.020 1.000 2 2010 2015
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2010 2010
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2010 2010
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2010 2010
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.030 1.000 3 2012 2018
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.030 1.000 3 2012 2018
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.030 1.000 3 2012 2018
Obsessive-Compulsive Disorder
CUI: C0028768
Disease: Obsessive-Compulsive Disorder
112 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.020 1.000 2 2012 2014
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2012 2012
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.030 1.000 3 2013 2018
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
176 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2013 2013
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2013 2013
Juvenile arthritis
CUI: C3495559
Disease: Juvenile arthritis
128 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2013 2013
Juvenile rheumatoid arthritis
CUI: C3714757
Disease: Juvenile rheumatoid arthritis
10 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2013 2013
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.020 1.000 2 2014 2014
Acute periodontitis
CUI: C0001342
Disease: Acute periodontitis
49 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2014 2014
Aggressive Periodontitis
CUI: C0031106
Disease: Aggressive Periodontitis
59 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2014 2014
Gilles de la Tourette syndrome
CUI: C0040517
Disease: Gilles de la Tourette syndrome
63 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2014 2014
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2014 2014
Intracranial Aneurysm
CUI: C0007766
Disease: Intracranial Aneurysm
150 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.020 1.000 2 2015 2017
Complications of Diabetes Mellitus
CUI: C0342257
Disease: Complications of Diabetes Mellitus
35 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2015 2015