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: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.030 1.000 3 2012 2018
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.030 1.000 3 2013 2018
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.030 1.000 3 2018 2019
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		0.030 1.000 3 2018 2019
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.030 1.000 3 2012 2018
dbSNP: rs745738344
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.030 0.333 3 2010 2014
dbSNP: rs1799724
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.020 1.000 2 2015 2017
dbSNP: rs1799724
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.020 0.500 2 2014 2014
dbSNP: rs1799724
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.020 1.000 2 2015 2017
dbSNP: rs1799964
rs1799964
LTA ; TNF ; LOC100287329
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		0.020 1.000 2 2013 2019
dbSNP: rs1799964
rs1799964
LTA ; TNF ; LOC100287329
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.020 1.000 2 2013 2014
dbSNP: rs1799964
rs1799964
LTA ; TNF ; LOC100287329
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0011311
Disease: Dengue Fever
Dengue Fever 		0.020 1.000 2 2013 2015
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		0.020 1.000 2 2012 2019
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive 		0.020 1.000 2 2011 2019
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		0.020 1.000 2 2013 2013
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		0.020 1.000 2 2015 2019
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0015672
Disease: Fatigue
Fatigue 		0.020 1.000 2 2009 2012
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.020 1.000 2 2016 2019
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.020 0.500 2 2014 2015
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C4721806
Disease: Carcinoma, Basal Cell
Carcinoma, Basal Cell 		0.020 1.000 2 2011 2017
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		0.020 1.000 2 2018 2019
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.020 1.000 2 2014 2018
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.020 0.500 2 2015 2016
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0079731
Disease: B-Cell Lymphomas
B-Cell Lymphomas 		0.020 1.000 2 2012 2013
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		0.020 1.000 2 2016 2019