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.
AA amyloidosis
CUI: C3536715
Disease: AA amyloidosis
10 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2011 2011
Active tuberculosis
CUI: C0151332
Disease: Active tuberculosis
25 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.020 1.000 2 2007 2010
Acute bronchiolitis
CUI: C0001311
Disease: Acute bronchiolitis
3 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1 2015 2015
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
Acute leukemia
CUI: C0085669
Disease: Acute leukemia
50 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2013 2013
Acute Motor Axonal Neuropathy
CUI: C3890941
Disease: Acute Motor Axonal Neuropathy
4 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2010 2010
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2007 2007
Acute pancreatitis
CUI: C0001339
Disease: Acute pancreatitis
51 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.030 0.667 3 2007 2014
Acute periodontitis
CUI: C0001342
Disease: Acute periodontitis
49 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.020 1.000 2 2008 2015
Acute pyelonephritis
CUI: C0520575
Disease: Acute pyelonephritis
10 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2018 2018
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2011 2011
Adrenoleukodystrophy
CUI: C0162309
Disease: Adrenoleukodystrophy
116 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2013 2013
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
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.040 0.250 4 2005 2009
Aggressive Periodontitis
CUI: C0031106
Disease: Aggressive Periodontitis
59 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.020 1.000 2 2008 2015
Allergic asthma
CUI: C0155877
Disease: Allergic asthma
55 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.020 1.000 2 2004 2020
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
176 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2012 2012
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
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
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2019 2019
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
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.760 0.571 7 2005 2018
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
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.090 0.778 9 2002 2012
Arthritis
CUI: C0003864
Disease: Arthritis
69 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2017 2017