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: 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: rs1799724
rs1799724 		0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02
CUI: C1321756
Disease: Achalasia
Achalasia 		0.010 1.000 1 2014 2014
dbSNP: rs1800629
rs1800629 		0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		Infections; Immune System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs3093662
rs3093662 		0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		Infections; Immune System Diseases 0.700 1.000 1 2009 2009
dbSNP: rs3093661
rs3093661 		1.000 6 31575981 intron variant G/A snv 3.5E-02
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 2 2009 2010
dbSNP: rs3093662
rs3093662 		0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 2 2009 2010
dbSNP: rs3093668
rs3093668 		1.000 6 31578718 downstream gene variant G/C snv 3.5E-02
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2009 2009
dbSNP: rs1800629
rs1800629 		0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C2215101
Disease: Acute cerebral ischemia
Acute cerebral ischemia 		Nervous System Diseases; 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: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic 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: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs361525
rs361525 		0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease 		Immune System 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: C0001339
Disease: Acute pancreatitis
Acute pancreatitis 		Digestive System Diseases 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: C0001342
Disease: Acute periodontitis
Acute periodontitis 		Stomatognathic Diseases 0.020 1.000 2 2014 2016
dbSNP: rs1800630
rs1800630 		0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis 		Stomatognathic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs361525
rs361525 		0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis 		Stomatognathic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1799724
rs1799724 		0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma 		Neoplasms 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: C0279628
Disease: Adenocarcinoma Of Esophagus
Adenocarcinoma Of Esophagus 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2016 2016
dbSNP: rs1800629
rs1800629 		0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1800630
rs1800630 		0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.010 1.000 1 2019 2019
dbSNP: rs361525
rs361525 		0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 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: C0031106
Disease: Aggressive Periodontitis
Aggressive Periodontitis 		Stomatognathic Diseases 0.020 1.000 2 2014 2016
dbSNP: rs1800630
rs1800630 		0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14
CUI: C0031106
Disease: Aggressive Periodontitis
Aggressive Periodontitis 		Stomatognathic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs361525
rs361525 		0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0031106
Disease: Aggressive Periodontitis
Aggressive Periodontitis 		Stomatognathic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs3093661
rs3093661 		1.000 6 31575981 intron variant G/A snv 3.5E-02
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 2 2009 2010
dbSNP: rs3093662
rs3093662 		0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 2 2009 2010