rs1800775, CETP

N. diseases: 18
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.800 1.000 11 2007 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.800 1.000 3 2012 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.710 1.000 2 2013 2018
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.700 1.000 5 2008 2013
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.700 1.000 2 2007 2009
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.700 1.000 1 2011 2011
Lipids measurement
CUI: C0523744
Disease: Lipids measurement
53 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.700 1.000 1 2009 2009
Pseudocholinesterase Measurement
CUI: C1168443
Disease: Pseudocholinesterase Measurement
568 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.700 1.000 1 2011 2011
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.700 1.000 1 2012 2012
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.020 1.000 2 2017 2019
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.010 1.000 1 2012 2012
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.010 1.000 1 2013 2013
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.010 1.000 1 2019 2019
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.010 1.000 1 2019 2019
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.010 1.000 1 2015 2015
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.010 1.000 1 2017 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.010 1.000 1 2014 2014
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.010 1.000 1 2009 2009