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: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0338480
Disease: Common Migraine
Common Migraine 		0.010 1.000 1 2009 2009
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0006060
Disease: Boutonneuse Fever
Boutonneuse Fever 		0.010 1.000 1 2009 2009
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0037317
Disease: Sleep disturbances
Sleep disturbances 		0.010 1.000 1 2009 2009
dbSNP: rs1800750
rs1800750
TNF
0.827 0.280 6 31575186 upstream gene variant G/A snv 1.6E-02
CUI: C0338480
Disease: Common Migraine
Common Migraine 		0.010 1.000 1 2009 2009
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0206368
Disease: Exfoliation Syndrome
Exfoliation Syndrome 		0.010 1.000 1 2009 2009
dbSNP: rs673
rs673
TNF
0.882 0.080 6 31575318 upstream gene variant G/A snv 1.8E-02
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.010 1.000 1 2009 2009
dbSNP: rs745738344
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		0.010 1.000 1 2009 2009
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.040 1.000 4 2010 2019
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.030 1.000 3 2010 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: rs1800630
rs1800630
LTA ; TNF ; LOC100287329
0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.020 1.000 2 2010 2015
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.020 1.000 2 2010 2015
dbSNP: rs1799964
rs1799964
LTA ; TNF ; LOC100287329
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2010 2010
dbSNP: rs1799964
rs1799964
LTA ; TNF ; LOC100287329
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.010 1.000 1 2010 2010
dbSNP: rs1799964
rs1799964
LTA ; TNF ; LOC100287329
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C0553694
Disease: Oropharyngeal disorders
Oropharyngeal disorders 		0.010 1.000 1 2010 2010
dbSNP: rs1799964
rs1799964
LTA ; TNF ; LOC100287329
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		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: 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: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2010 2010
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.010 1.000 1 2010 2010
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.010 1.000 1 2010 2010
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0079772
Disease: T-Cell Lymphoma
T-Cell Lymphoma 		0.010 1.000 1 2010 2010
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C4721414
Disease: Mantle cell lymphoma
Mantle cell lymphoma 		0.010 1.000 1 2010 2010
dbSNP: rs1800629
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14
CUI: C0334634
Disease: Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse
Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse 		0.010 1.000 1 2010 2010
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2010 2010
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.010 1.000 1 2010 2010