Source: ALL

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: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis 		0.010 1.000 1 2018 2018
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.010 1.000 1 2012 2012
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0036690
Disease: Septicemia
Septicemia 		0.010 1.000 1 2017 2017
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
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0342257
Disease: Complications of Diabetes Mellitus
Complications of Diabetes Mellitus 		0.010 1.000 1 2015 2015
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C1456868
Disease: Diabetic foot ulcer
Diabetic foot ulcer 		0.010 1.000 1 2018 2018
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 2016 2016
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0003857
Disease: Congenital arteriovenous malformation
Congenital arteriovenous malformation 		0.010 1.000 1 2018 2018
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease 		0.010 1.000 1 2017 2017
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0023343
Disease: Leprosy
Leprosy 		0.010 1.000 1 2015 2015
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis 		0.010 1.000 1 2013 2013
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2016 2016
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 < 0.001 1 2016 2016
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		0.010 1.000 1 2013 2013
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0004606
Disease: Nonproliferative diabetic retinopathy
Nonproliferative diabetic retinopathy 		0.010 1.000 1 2016 2016
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 < 0.001 1 2016 2016
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C1609538
Disease: Latent Tuberculosis
Latent Tuberculosis 		0.010 1.000 1 2019 2019
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: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		0.010 1.000 1 2016 2016
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C3714757
Disease: Juvenile rheumatoid arthritis
Juvenile rheumatoid arthritis 		0.010 1.000 1 2013 2013
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C4721806
Disease: Carcinoma, Basal Cell
Carcinoma, Basal Cell 		0.010 1.000 1 2017 2017
dbSNP: rs361525
rs361525
TNF
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 		0.010 1.000 1 2019 2019
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0032463
Disease: Polycythemia Vera
Polycythemia Vera 		0.010 1.000 1 2019 2019
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C3811653
Disease: Experimental Organism Basal Cell Carcinoma
Experimental Organism Basal Cell Carcinoma 		0.010 1.000 1 2017 2017