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: 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: rs4986791
rs4986791
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.010 1.000 1 2003 2003
dbSNP: rs4986791
rs4986791
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 1.000 1 2003 2003
dbSNP: rs1191926239
rs1191926239
0.807 0.200 9 117704539 missense variant C/G snv 4.0E-06
CUI: C0003615
Disease: Appendicitis
Appendicitis
0.010 1.000 1 2004 2004
dbSNP: rs1191926239
rs1191926239
0.807 0.200 9 117704539 missense variant C/G snv 4.0E-06
CUI: C0017086
Disease: Gangrene
Gangrene
0.010 1.000 1 2004 2004
dbSNP: rs200527106
rs200527106
0.925 0.120 9 117712902 missense variant G/A;C snv 4.0E-06
CUI: C0456103
Disease: Sepsis of the newborn
Sepsis of the newborn
0.010 1.000 1 2004 2004
dbSNP: rs200527106
rs200527106
0.925 0.120 9 117712902 missense variant G/A;C snv 4.0E-06
CUI: C3665339
Disease: Bacterial sepsis of newborn
Bacterial sepsis of newborn
0.010 1.000 1 2004 2004
dbSNP: rs200527106
rs200527106
0.925 0.120 9 117712902 missense variant G/A;C snv 4.0E-06
CUI: C0282666
Disease: Very Low Birth Weight
Very Low Birth Weight
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: 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
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: 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: 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: 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
Diabetes Mellitus, Insulin-Dependent
0.010 1.000 1 2004 2004
dbSNP: rs4986791
rs4986791
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.010 < 0.001 1 2004 2004
dbSNP: rs4986791
rs4986791
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
CUI: C0011882
Disease: Diabetic Neuropathies
Diabetic Neuropathies
0.010 1.000 1 2004 2004
dbSNP: rs754342091
rs754342091
0.790 0.200 9 117712421 missense variant A/G snv 3.2E-05 1.4E-05
CUI: C0017086
Disease: Gangrene
Gangrene
0.010 1.000 1 2004 2004
dbSNP: rs754342091
rs754342091
0.790 0.200 9 117712421 missense variant A/G snv 3.2E-05 1.4E-05
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: 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: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.020 0.500 2 2005 2005
dbSNP: rs1371329921
rs1371329921
0.925 0.080 9 117712993 stop gained C/T snv 4.0E-06 1.4E-05
CUI: C0238013
Disease: Invasive aspergillosis
Invasive aspergillosis
0.010 1.000 1 2005 2005