Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1800610
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2008 2008
dbSNP: rs1800610
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.010 1.000 1 2010 2010
dbSNP: rs1800610
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		0.010 1.000 1 2017 2017
dbSNP: rs1800610
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2008 2008
dbSNP: rs1800610
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02
CUI: C0030193
Disease: Pain
Pain 		0.010 1.000 1 2017 2017
dbSNP: rs1800610
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2010 2010
dbSNP: rs3093662
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02
CUI: C0003467
Disease: Anxiety
Anxiety 		0.010 1.000 1 2016 2016
dbSNP: rs3093662
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		0.010 1.000 1 2011 2011
dbSNP: rs3093662
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders 		0.010 1.000 1 2016 2016
dbSNP: rs3093664
rs3093664
TNF
6 31576865 intron variant A/G snv 6.9E-02 7.7E-02
CUI: C0043144
Disease: Wheezing
Wheezing 		0.010 1.000 1 2016 2016
dbSNP: rs1232013698
rs1232013698
TNF
6 31577208 missense variant G/T snv 4.1E-06
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		0.010 1.000 1 2009 2009
dbSNP: rs1250554906
rs1250554906
TNF
1.000 0.120 6 31576808 missense variant G/A snv 4.1E-06 7.0E-06
CUI: C0393814
Disease: Hereditary liability to pressure palsies
Hereditary liability to pressure palsies 		0.010 1.000 1 2014 2014
dbSNP: rs1250915035
rs1250915035
TNF
0.925 6 31576537 missense variant C/T snv 4.0E-06
CUI: C0374997
Disease: Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site 		0.010 1.000 1 2017 2017
dbSNP: rs1250915035
rs1250915035
TNF
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: rs1411364031
rs1411364031
TNF
0.882 0.040 6 31577502 missense variant T/C snv 7.0E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2014 2014
dbSNP: rs1411364031
rs1411364031
TNF
0.882 0.040 6 31577502 missense variant T/C snv 7.0E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2014 2014
dbSNP: rs1411364031
rs1411364031
TNF
0.882 0.040 6 31577502 missense variant T/C snv 7.0E-06
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 2014 2014
dbSNP: rs1418646618
rs1418646618
TNF
1.000 0.080 6 31575843 missense variant C/G snv 1.2E-05 7.0E-06
CUI: C0024534
Disease: Malaria, Cerebral
Malaria, Cerebral 		0.010 1.000 1 2013 2013
dbSNP: rs1454071630
rs1454071630
TNF
1.000 0.040 6 31577259 missense variant G/A;T snv 8.1E-06
CUI: C0343055
Disease: Generalized pustular psoriasis
Generalized pustular psoriasis 		0.010 1.000 1 2012 2012
dbSNP: rs35131721
rs35131721
TNF
1.000 0.080 6 31576538 missense variant C/T snv 3.2E-05 2.8E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs370893734
rs370893734
TNF
1.000 0.200 6 31577481 missense variant G/A;T snv 2.0E-05; 1.6E-05
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.010 1.000 1 2007 2007
dbSNP: rs4645843
rs4645843
TNF
1.000 0.120 6 31576785 missense variant C/G;T snv 2.6E-03
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.010 1.000 1 2017 2017
dbSNP: rs548532642
rs548532642
TNF
0.882 0.080 6 31577184 missense variant G/A;T snv 1.6E-05
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2006 2006
dbSNP: rs548532642
rs548532642
TNF
0.882 0.080 6 31577184 missense variant G/A;T snv 1.6E-05
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2006 2006
dbSNP: rs548532642
rs548532642
TNF
0.882 0.080 6 31577184 missense variant G/A;T snv 1.6E-05
CUI: C1304140
Disease: Familial psoriasis
Familial psoriasis 		0.010 1.000 1 2012 2012