rs4986790, TLR4

N. diseases: 146
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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
956 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.800 0.833 13 2004 2017
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
696 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.780 0.875 9 2004 2017
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
121 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.070 0.571 7 2002 2012
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
131 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.070 0.571 7 2002 2012
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
454 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.070 0.714 7 2005 2007
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
11 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.070 0.857 7 2004 2015
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
422 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.750 0.400 6 2005 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.060 0.667 6 2003 2005
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
451 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.060 0.833 6 2004 2016
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
1878 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.060 0.500 6 2006 2015
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
364 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.060 1.000 6 2007 2013
Diabetes Mellitus, Non-Insulin-Dependent
1522 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.050 0.800 5 2004 2018
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
341 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.050 1.000 5 2007 2013
Sepsis
CUI: C0243026
Disease: Sepsis
63 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.050 1.000 5 2002 2015
Septicemia
CUI: C0036690
Disease: Septicemia
63 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.050 1.000 5 2002 2015
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
551 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.040 0.250 4 2005 2009
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
41 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.040 0.750 4 2004 2007
Colorectal Cancer
CUI: C1527249
Disease: Colorectal Cancer
955 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.040 1.000 4 2006 2016
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
539 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.040 1.000 4 2006 2016
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
189 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.040 0.750 4 2003 2005
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
861 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.040 0.750 4 2003 2005
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
124 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.040 1.000 4 2005 2016
Acute pancreatitis
CUI: C0001339
Disease: Acute pancreatitis
20 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.030 0.667 3 2007 2015
Asthma
CUI: C0004096
Disease: Asthma
729 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.030 0.667 3 2004 2010
Bacterial Infections
CUI: C0004623
Disease: Bacterial Infections
11 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.030 0.667 3 2006 2011