Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1458766475
rs1458766475
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.090 0.889 9 1997 2014
dbSNP: rs5361
rs5361
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.090 0.889 9 1997 2014
dbSNP: rs1458766475
rs1458766475
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.040 0.750 4 1998 2014
dbSNP: rs5361
rs5361
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.040 0.750 4 1998 2014
dbSNP: rs5361
rs5361
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
Cardiovascular Diseases 0.070 1.000 7 1999 2019
dbSNP: rs5361
rs5361
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
Cardiovascular Diseases 0.070 1.000 7 1999 2019
dbSNP: rs1458766475
rs1458766475
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
Cardiovascular Diseases 0.060 1.000 6 1999 2012
dbSNP: rs1458766475
rs1458766475
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
Cardiovascular Diseases 0.060 1.000 6 1999 2012
dbSNP: rs5355
rs5355
0.742 0.240 1 169726729 missense variant G/A snv 4.5E-02 3.3E-02
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
Cardiovascular Diseases 0.020 1.000 2 1999 2019
dbSNP: rs5355
rs5355
0.742 0.240 1 169726729 missense variant G/A snv 4.5E-02 3.3E-02
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
Cardiovascular Diseases 0.020 1.000 2 1999 2019
dbSNP: rs1131498
rs1131498
0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2000 2000
dbSNP: rs1131498
rs1131498
0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22
CUI: C0011847
Disease: Diabetes
Diabetes
Endocrine System Diseases 0.010 1.000 1 2000 2000
dbSNP: rs1131498
rs1131498
0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2000 2000
dbSNP: rs5361
rs5361
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.080 0.875 8 2001 2011
dbSNP: rs1458766475
rs1458766475
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.070 0.857 7 2001 2009
dbSNP: rs1458766475
rs1458766475
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.050 0.800 5 2003 2009
dbSNP: rs5361
rs5361
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.050 0.800 5 2003 2009
dbSNP: rs1458766475
rs1458766475
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.030 1.000 3 2003 2009
dbSNP: rs5361
rs5361
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.030 1.000 3 2003 2009
dbSNP: rs1458766475
rs1458766475
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 0.500 2 2003 2007
dbSNP: rs5361
rs5361
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 0.500 2 2003 2007
dbSNP: rs1458766475
rs1458766475
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06
Premature coronary artery atherosclerosis
Cardiovascular Diseases 0.010 1.000 1 2003 2003
dbSNP: rs2229569
rs2229569
0.790 0.360 1 169704697 missense variant G/A;T snv 0.21; 3.2E-05
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.010 < 0.001 1 2003 2003
dbSNP: rs5361
rs5361
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02
Premature coronary artery atherosclerosis
Cardiovascular Diseases 0.010 1.000 1 2003 2003
dbSNP: rs1458766475
rs1458766475
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06
CUI: C0852949
Disease: Arteriopathic disease
Arteriopathic disease
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2004 2004