rs1800629, TNF

N. diseases: 169
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.
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
CUI: C0375023
Disease: Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
14 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2009 2009
Diabetic foot ulcer
CUI: C1456868
Disease: Diabetic foot ulcer
17 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2018 2018
Mantle cell lymphoma
CUI: C4721414
Disease: Mantle cell lymphoma
19 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2010 2010
Classical Hodgkin's Lymphoma
CUI: C1333064
Disease: Classical Hodgkin's Lymphoma
20 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2013 2013
Tuberculosis, extrapulmonary
CUI: C0679362
Disease: Tuberculosis, extrapulmonary
21 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2011 2011
Precursor B-cell lymphoblastic leukemia
CUI: C1292769
Disease: Precursor B-cell lymphoblastic leukemia
23 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2014 2014
Spondylarthritis
CUI: C0949690
Disease: Spondylarthritis
23 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2018 2018
T-Cell Lymphoma
CUI: C0079772
Disease: T-Cell Lymphoma
24 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2010 2010
Endothelial dysfunction
CUI: C0856169
Disease: Endothelial dysfunction
25 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2012 2012
Peptic Ulcer
CUI: C0030920
Disease: Peptic Ulcer
25 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2014 2014
Severe Dengue
CUI: C0019100
Disease: Severe Dengue
25 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2013 2013
Temporomandibular Joint Disorders
CUI: C0039494
Disease: Temporomandibular Joint Disorders
25 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2016 2016
Severe Sepsis
CUI: C1719672
Disease: Severe Sepsis
29 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.020 1.000 2 2012 2015
Cervical Intraepithelial Neoplasia
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
29 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2013 2013
Kidney Failure, Acute
CUI: C0022660
Disease: Kidney Failure, Acute
32 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.020 0.500 2 2013 2019
Aspirin exacerbated respiratory disease
CUI: C3853540
Disease: Aspirin exacerbated respiratory disease
32 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1 2017 2017
Bronchiolitis
CUI: C0006271
Disease: Bronchiolitis
32 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2009 2009
Caries (morphologic abnormality)
CUI: C0333519
Disease: Caries (morphologic abnormality)
33 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2017 2017
Pneumonia
CUI: C0032285
Disease: Pneumonia
33 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2015 2015
Rheumatic Heart Disease
CUI: C0035439
Disease: Rheumatic Heart Disease
33 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2016 2016
Nasal Polyps
CUI: C0027430
Disease: Nasal Polyps
34 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.020 1.000 2 2009 2018
Complications of Diabetes Mellitus
CUI: C0342257
Disease: Complications of Diabetes Mellitus
35 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2015 2015
Meniere Disease
CUI: C0025281
Disease: Meniere Disease
36 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2013 2013
Osteoporosis, Postmenopausal
CUI: C0029458
Disease: Osteoporosis, Postmenopausal
38 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2018 2018
Sleep Disorders
CUI: C0851578
Disease: Sleep Disorders
38 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2009 2009