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.
Erythema nodosum leprosum
CUI: C0343467
Disease: Erythema nodosum leprosum
1 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2016 2016
Reticuloendotheliosis, X-linked
CUI: C0035288
Disease: Reticuloendotheliosis, X-linked
1 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2017 2017
Type 2 lepra reaction
CUI: C0343466
Disease: Type 2 lepra reaction
1 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2016 2016
Acute cerebral ischemia
CUI: C2215101
Disease: Acute cerebral ischemia
2 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2016 2016
Recurrent mouth ulcers
CUI: C0554021
Disease: Recurrent mouth ulcers
2 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2013 2013
Septicaemia due to gram-negative organism, unspecified
2 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2014 2014
Boutonneuse Fever
CUI: C0006060
Disease: Boutonneuse Fever
3 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2009 2009
Centriacinar Emphysema
CUI: C0221227
Disease: Centriacinar Emphysema
3 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2013 2013
Cervical Squamous Intraepithelial Neoplasia
3 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2013 2013
Neck Pain
CUI: C0007859
Disease: Neck Pain
3 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2018 2018
Paraseptal emphysema
CUI: C0264394
Disease: Paraseptal emphysema
3 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2013 2013
Pemphigus
CUI: C0030807
Disease: Pemphigus
3 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2016 2016
Pneumoconiosis
CUI: C0032273
Disease: Pneumoconiosis
4 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2013 2013
Visually threatening diabetic retinopathy
4 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1 2016 2016
Japanese Encephalitis
CUI: C0014057
Disease: Japanese Encephalitis
6 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2019 2019
Mesial temporal lobe epilepsy with hippocampal sclerosis
7 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2018 2018
Candidiasis
CUI: C0006840
Disease: Candidiasis
8 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2014 2014
Heart Failure, Diastolic
CUI: C1135196
Disease: Heart Failure, Diastolic
9 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2017 2017
Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse
9 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2010 2010
Systemic Inflammatory Response Syndrome
9 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2008 2008
Dyssomnias
CUI: C0700201
Disease: Dyssomnias
10 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2009 2009
Spindle cell hemangioma
CUI: C1304508
Disease: Spindle cell hemangioma
10 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2008 2008
Pancreatic Diseases
CUI: C0030286
Disease: Pancreatic Diseases
11 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1 2017 2017
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
Proliferative vitreoretinopathy
CUI: C0242852
Disease: Proliferative vitreoretinopathy
14 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2018 2018