TNF, tumor necrosis factor, 7124

N. diseases: 2724; N. variants: 31
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0003467
Disease: Anxiety
Anxiety
Behavior and Behavior Mechanisms 0.010 1.000 1 2016 2016
dbSNP: rs1800629
rs1800629
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0344315
Disease: Depressed mood
Depressed mood
Behavior and Behavior Mechanisms 0.010 1.000 1 2019 2019
dbSNP: rs1800629
rs1800629
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0011570
Disease: Mental Depression
Mental Depression
Behavior and Behavior Mechanisms 0.010 1.000 1 2019 2019
dbSNP: rs1800629
rs1800629
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
Behavior and Behavior Mechanisms 0.010 1.000 1 2017 2017
dbSNP: rs3093662
rs3093662
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02
CUI: C0003467
Disease: Anxiety
Anxiety
Behavior and Behavior Mechanisms 0.010 1.000 1 2016 2016
dbSNP: rs1800629
rs1800629
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.030 0.667 3 2013 2019
dbSNP: rs1800629
rs1800629
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.020 0.500 2 2014 2018
dbSNP: rs1800629
rs1800629
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
Cardiovascular Diseases 0.020 1.000 2 2011 2016
dbSNP: rs1411364031
rs1411364031
0.882 0.040 6 31577502 missense variant T/C snv 7.0E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1411364031
rs1411364031
0.882 0.040 6 31577502 missense variant T/C snv 7.0E-06
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1411364031
rs1411364031
0.882 0.040 6 31577502 missense variant T/C snv 7.0E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1800629
rs1800629
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C1135196
Disease: Heart Failure, Diastolic
Heart Failure, Diastolic
Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1800629
rs1800629
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1800629
rs1800629
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1800629
rs1800629
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1800629
rs1800629
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1800629
rs1800629
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs361525
rs361525
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs361525
rs361525
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs361525
rs361525
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs745738344
rs745738344
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia
Cardiovascular Diseases 0.010 < 0.001 1 2005 2005