rs361525, TNF

N. diseases: 62
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2015 2015
Leprosy
CUI: C0023343
Disease: Leprosy
120 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2015 2015
Cerebral Palsy
CUI: C0007789
Disease: Cerebral Palsy
69 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2016 2016
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2016 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2016 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2016 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1 2016 2016
Nonproliferative diabetic retinopathy
CUI: C0004606
Disease: Nonproliferative diabetic retinopathy
1 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2016 2016
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1 2016 2016
Tuberculosis, Pulmonary
CUI: C0041327
Disease: Tuberculosis, Pulmonary
171 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2016 2016
Visually threatening diabetic retinopathy
CUI: C0339470
Disease: Visually threatening diabetic retinopathy
4 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1 2016 2016
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.020 1.000 2 2017 2018
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.020 1.000 2 2017 2018
Acute GVH disease
CUI: C0856825
Disease: Acute GVH disease
49 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2017 2017
Carcinoma, Basal Cell
CUI: C4721806
Disease: Carcinoma, Basal Cell
91 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2017 2017
Experimental Organism Basal Cell Carcinoma
CUI: C3811653
Disease: Experimental Organism Basal Cell Carcinoma
63 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2017 2017
melanoma
CUI: C0025202
Disease: melanoma
515 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2017 2017
Obesity
CUI: C0028754
Disease: Obesity
1111 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2017 2017
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2017 2017
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2017 2017
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2017 2017
Arthritis, Psoriatic
CUI: C0003872
Disease: Arthritis, Psoriatic
89 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.030 1.000 3 2018 2019
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.030 1.000 3 2018 2019
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.020 0.500 2 2018 2019
Bronchopulmonary Dysplasia
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
112 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2018 2018