rs4986790, TLR4

N. diseases: 223
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.
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2003 2003
Coronary Stenosis
CUI: C0242231
Disease: Coronary Stenosis
20 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1 2003 2003
Allergic rhinoconjunctivitis
CUI: C0861154
Disease: Allergic rhinoconjunctivitis
2 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2004 2004
Appendicitis
CUI: C0003615
Disease: Appendicitis
10 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2004 2004
Chlamydia Infections
CUI: C0008149
Disease: Chlamydia Infections
10 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1 2004 2004
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2004 2004
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1 2004 2004
Diabetic Neuropathies
CUI: C0011882
Disease: Diabetic Neuropathies
12 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2004 2004
Gangrene
CUI: C0017086
Disease: Gangrene
4 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2004 2004
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2004 2004
Vascular inflammations
CUI: C0947751
Disease: Vascular inflammations
3 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2004 2004
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.020 0.500 2 2005 2005
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.020 1.000 2 2003 2005
Atherothrombosis
CUI: C1963943
Disease: Atherothrombosis
15 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2005 2005
Bronchiolitis Obliterans
CUI: C0006272
Disease: Bronchiolitis Obliterans
5 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2005 2005
Gastric Mucosa-Associated Lymphoid Tissue Lymphoma
CUI: C1333782
Disease: Gastric Mucosa-Associated Lymphoid Tissue Lymphoma
1 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2005 2005
Generalized periodontitis
CUI: C4023560
Disease: Generalized periodontitis
5 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2005 2005
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2005 2005
Legionnaires' Disease
CUI: C0023241
Disease: Legionnaires' Disease
3 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2005 2005
Wheezing
CUI: C0043144
Disease: Wheezing
54 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2005 2005
Adult Hodgkin Lymphoma
CUI: C0220597
Disease: Adult Hodgkin Lymphoma
27 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2006 2006
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2006 2006
Anemia
CUI: C0002871
Disease: Anemia
94 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1 2006 2006
Arthritis, Reactive
CUI: C0085435
Disease: Arthritis, Reactive
2 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1 2006 2006
Candidemia
CUI: C0877445
Disease: Candidemia
11 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2006 2006