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: rs3093661
rs3093661
1.000 6 31575981 intron variant G/A snv 3.5E-02
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.700 1.000 2 2009 2010
dbSNP: rs3093661
rs3093661
1.000 6 31575981 intron variant G/A snv 3.5E-02
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
0.700 1.000 2 2009 2010
dbSNP: rs3093661
rs3093661
1.000 6 31575981 intron variant G/A snv 3.5E-02
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.700 1.000 2 2009 2010
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
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: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE 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
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY 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
dbSNP: rs1250915035
rs1250915035
0.925 6 31576537 missense variant C/T snv 4.0E-06
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
0.010 1.000 1 2017 2017
dbSNP: rs1250915035
rs1250915035
0.925 6 31576537 missense variant C/T snv 4.0E-06
CUI: C3826128
Disease: Infection in children
Infection in children
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: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0549523
Disease: Oropharynx (excludes nasopharynx)
Oropharynx (excludes nasopharynx)
0.010 1.000 1 2013 2013
dbSNP: rs1799964
rs1799964
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C1096197
Disease: Immune reconstitution syndrome
Immune reconstitution syndrome
0.010 1.000 1 2013 2013
dbSNP: rs1800629
rs1800629
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
0.010 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: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction
0.010 1.000 1 2012 2012
dbSNP: rs3093664
rs3093664
6 31576865 intron variant A/G snv 6.9E-02 7.7E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs3093668
rs3093668
1.000 6 31578718 downstream gene variant G/C snv 3.5E-02
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
0.700 1.000 1 2009 2009
dbSNP: rs3093668
rs3093668
1.000 6 31578718 downstream gene variant G/C snv 3.5E-02
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.700 1.000 1 2009 2009
dbSNP: rs3093668
rs3093668
1.000 6 31578718 downstream gene variant G/C snv 3.5E-02
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.700 1.000 1 2009 2009
dbSNP: rs3093668
rs3093668
1.000 6 31578718 downstream gene variant G/C snv 3.5E-02
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
0.700 1.000 1 2009 2009
dbSNP: rs745738344
rs745738344
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05
CUI: C1335059
Disease: testicular nonseminoma
testicular nonseminoma
0.010 1.000 1 2007 2007
dbSNP: rs1799724
rs1799724
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02
VASCULAR DEMENTIA, SUSCEPTIBILITY TO
0.700 0
dbSNP: rs1799724
rs1799724
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02
ALZHEIMER DISEASE, SUSCEPTIBILITY TO
0.700 0
dbSNP: rs281865419
rs281865419
6 31577157 missense variant C/T snv 8.1E-06 7.0E-06
CUI: C4016415
Disease: TNF RECEPTOR BINDING, ALTERED
TNF RECEPTOR BINDING, ALTERED
0.700 0
dbSNP: rs1800629
rs1800629
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms
Behavior and Behavior Mechanisms 0.020 1.000 2 2015 2019