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.
Childhood Hodgkin Lymphoma
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
29 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
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 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
Infected pancreatic necrosis
CUI: C0341479
Disease: Infected pancreatic necrosis
2 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1 2006 2006
Mucosa-Associated Lymphoid Tissue Lymphoma
CUI: C0242647
Disease: Mucosa-Associated Lymphoid Tissue Lymphoma
13 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
Neonatal disorder
CUI: C0021290
Disease: Neonatal disorder
4 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
Osteomyelitis
CUI: C0029443
Disease: Osteomyelitis
14 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
Pancreatitis
CUI: C0030305
Disease: Pancreatitis
80 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1 2006 2006
Spondylarthropathies
CUI: C0949691
Disease: Spondylarthropathies
7 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
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.040 0.750 4 2003 2007
Respiratory Syncytial Virus Infections
CUI: C0035235
Disease: Respiratory Syncytial Virus Infections
5 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.020 1.000 2 2006 2007
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
Atherosclerosis of aorta
CUI: C0155733
Disease: Atherosclerosis of aorta
1 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1 2007 2007
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 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
Cystic Fibrosis
CUI: C0010674
Disease: Cystic Fibrosis
704 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
Intestinal metaplasia
CUI: C0334037
Disease: Intestinal metaplasia
24 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1 2007 2007
Mycobacterium Infections
CUI: C0026918
Disease: Mycobacterium Infections
14 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
Necrosis of pancreas
CUI: C0267953
Disease: Necrosis of pancreas
1 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
Pancreatic Infection
CUI: C0948160
Disease: Pancreatic Infection
1 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
precancerous lesions
CUI: C0940937
Disease: precancerous lesions
19 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
Renal vascular disorder
CUI: C0268790
Disease: Renal vascular disorder
6 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
Endotoxin Hyporesponsiveness
CUI: C1864267
Disease: Endotoxin Hyporesponsiveness
2 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.020 1.000 2 2005 2008
Bronchopulmonary Aspergillosis
CUI: C2350530
Disease: Bronchopulmonary Aspergillosis
4 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2008 2008
Fetal Growth Retardation
CUI: C0015934
Disease: Fetal Growth Retardation
21 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2008 2008
Gram-negative bacteremia
CUI: C0744471
Disease: Gram-negative bacteremia
2 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2008 2008
HELLP Syndrome
CUI: C0162739
Disease: HELLP Syndrome
10 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2008 2008