Source: ALL

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: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.030 1.000 3 2004 2018
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0011847
Disease: Diabetes
Diabetes
0.030 1.000 3 2004 2018
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0155877
Disease: Allergic asthma
Allergic asthma
0.020 1.000 2 2004 2020
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C1827849
Disease: IgE-mediated allergic asthma
IgE-mediated allergic asthma
0.020 1.000 2 2004 2020
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
0.020 1.000 2 2004 2010
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0003615
Disease: Appendicitis
Appendicitis
0.010 1.000 1 2004 2004
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0947751
Disease: Vascular inflammations
Vascular inflammations
0.010 1.000 1 2004 2004
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0011882
Disease: Diabetic Neuropathies
Diabetic Neuropathies
0.010 1.000 1 2004 2004
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0008149
Disease: Chlamydia Infections
Chlamydia Infections
0.010 < 0.001 1 2004 2004
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.010 < 0.001 1 2004 2004
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0861154
Disease: Allergic rhinoconjunctivitis
Allergic rhinoconjunctivitis
0.010 1.000 1 2004 2004
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
Diabetes Mellitus, Insulin-Dependent
0.010 1.000 1 2004 2004
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0017086
Disease: Gangrene
Gangrene
0.010 1.000 1 2004 2004
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial
0.010 1.000 1 2004 2004
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 7 2005 2018
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
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: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.040 0.250 4 2005 2009
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C1864267
Disease: Endotoxin Hyporesponsiveness
Endotoxin Hyporesponsiveness
0.020 1.000 2 2005 2008
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis
0.020 0.500 2 2005 2015
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.020 0.500 2 2005 2005
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0043144
Disease: Wheezing
Wheezing
0.010 1.000 1 2005 2005
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
Gastric Mucosa-Associated Lymphoid Tissue Lymphoma
0.010 1.000 1 2005 2005
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0023241
Disease: Legionnaires' Disease
Legionnaires' Disease
0.010 1.000 1 2005 2005
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C4023560
Disease: Generalized periodontitis
Generalized periodontitis
0.010 1.000 1 2005 2005