Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 0.895 18 2004 2017
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.800 0.923 12 2004 2017
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.760 0.571 6 2005 2018
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.710 1.000 1 2016 2016
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.100 0.917 12 2004 2019
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.100 1.000 11 2007 2019
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.100 0.545 11 2004 2015
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.100 1.000 10 2007 2019
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0243026
Disease: Sepsis
Sepsis
0.090 0.889 9 2002 2016
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.090 0.778 9 2002 2012
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
0.090 0.778 9 2004 2015
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0031099
Disease: Periodontitis
Periodontitis
0.090 0.778 9 2004 2019
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0036690
Disease: Septicemia
Septicemia
0.090 0.889 9 2002 2016
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.090 0.778 9 2002 2012
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.080 0.750 8 2004 2014
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.080 0.875 8 2003 2019
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0004096
Disease: Asthma
Asthma
0.080 0.750 8 2004 2020
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.080 0.625 8 2003 2017
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.070 0.714 7 2006 2018
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.060 1.000 6 2006 2015
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.060 1.000 6 2006 2015
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary
0.060 1.000 6 2004 2019
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.060 0.833 6 2003 2017
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
0.060 0.833 6 2005 2016
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.060 0.833 6 2005 2019