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: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
0.010 1.000 1 2003 2003
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0242231
Disease: Coronary Stenosis
Coronary Stenosis
0.010 < 0.001 1 2003 2003
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: 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: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.020 1.000 2 2003 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
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C1963943
Disease: Atherothrombosis
Atherothrombosis
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: C0948008
Disease: Ischemic stroke
Ischemic stroke
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: C0006272
Disease: Bronchiolitis Obliterans
Bronchiolitis Obliterans
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: C0029443
Disease: Osteomyelitis
Osteomyelitis
0.010 1.000 1 2006 2006
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0949691
Disease: Spondylarthropathies
Spondylarthropathies
0.010 1.000 1 2006 2006
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
Mucosa-Associated Lymphoid Tissue Lymphoma
0.010 1.000 1 2006 2006
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0002871
Disease: Anemia
Anemia
0.010 < 0.001 1 2006 2006
dbSNP: rs4986790
rs4986790
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0030305
Disease: Pancreatitis
Pancreatitis
0.010 < 0.001 1 2006 2006