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: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		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: C4048328
Disease: cervical cancer
cervical cancer 		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: 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: 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: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.020 1.000 2 2017 2018
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.020 1.000 2 2007 2014
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: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.020 1.000 2 2007 2014
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.020 1.000 2 2017 2018
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.020 0.500 2 2006 2008
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm 		0.020 1.000 2 2015 2017
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0028768
Disease: Obsessive-Compulsive Disorder
Obsessive-Compulsive Disorder 		0.020 1.000 2 2012 2014
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.020 0.500 2 2018 2019
dbSNP: rs361525
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.020 1.000 2 2014 2014
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