rs1800629, TNF

N. diseases: 169
Source: BEFREE ×
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.
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
14 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2015 2015
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
Nasal Polyps
CUI: C0027430
Disease: Nasal Polyps
18 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.020 1.000 2 2009 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
Temporomandibular Joint Disorders
CUI: C0039494
Disease: Temporomandibular Joint Disorders
21 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2016 2016
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
Severe Dengue
CUI: C0019100
Disease: Severe Dengue
22 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2013 2013
Pneumonia
CUI: C0032285
Disease: Pneumonia
23 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2015 2015
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
Osteoporosis, Postmenopausal
CUI: C0029458
Disease: Osteoporosis, Postmenopausal
25 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2018 2018
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
Rheumatic Heart Disease
CUI: C0035439
Disease: Rheumatic Heart Disease
27 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
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
Sleep disturbances
CUI: C0037317
Disease: Sleep disturbances
33 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2009 2009
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