rs4986790, TLR4

N. diseases: 221
Source: BEFREE ×
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
456 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.800 0.895 18 2004 2017
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
392 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.800 0.923 12 2004 2017
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
273 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.760 0.571 6 2005 2018
Psoriasis
CUI: C0033860
Disease: Psoriasis
238 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.710 1.000 1 2016 2016
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
277 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.100 0.917 12 2004 2019
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
676 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.100 0.545 11 2004 2015
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
616 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.100 1.000 11 2007 2019
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
603 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.100 1.000 10 2007 2019
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
266 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
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
271 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
Periodontitis
CUI: C0031099
Disease: Periodontitis
90 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.090 0.778 9 2004 2019
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
14 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.090 0.778 9 2004 2015
Sepsis
CUI: C0243026
Disease: Sepsis
139 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.090 0.889 9 2002 2016
Septicemia
CUI: C0036690
Disease: Septicemia
139 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.090 0.889 9 2002 2016
Asthma
CUI: C0004096
Disease: Asthma
714 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.080 0.750 8 2004 2020
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1022 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.080 0.875 8 2003 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
769 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.080 0.625 8 2003 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
547 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.080 0.750 8 2004 2014
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1186 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.070 0.714 7 2006 2018
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
382 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.060 0.833 6 2005 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.060 0.833 6 2003 2017
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
24 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.060 0.833 6 2005 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1441 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.060 1.000 6 2006 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.060 1.000 6 2006 2015
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
306 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.060 0.833 6 2004 2016