rs2303790, CETP

N. diseases: 19
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.
HYPERALPHALIPOPROTEINEMIA 1
CUI: C3149462
Disease: HYPERALPHALIPOPROTEINEMIA 1
4 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.710 1.000 4 1990 2002
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.700 1.000 2 2018 2019
Exudative age-related macular degeneration
CUI: C0271084
Disease: Exudative age-related macular degeneration
109 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.700 1.000 1 2015 2015
exudative macular degeneration
CUI: C2237660
Disease: exudative macular degeneration
69 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.700 1.000 1 2015 2015
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.700 1.000 1 2012 2012
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.700 1.000 1 2012 2012
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.700 1.000 1 2018 2018
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.700 1.000 1 2012 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.030 1.000 3 1996 2005
Vascular Diseases
CUI: C0042373
Disease: Vascular Diseases
40 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.030 0.667 3 1999 2018
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.020 1.000 2 2015 2018
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.010 1.000 1 2008 2008
Cholesteryl Ester Transfer Protein Deficiency
CUI: C0342883
Disease: Cholesteryl Ester Transfer Protein Deficiency
5 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.010 1.000 1 2000 2000
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.010 1.000 1 2002 2002
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.010 1.000 1 2002 2002
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.010 1.000 1 1997 1997
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.010 1.000 1 1997 1997
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.010 1.000 1 2002 2002
Polypoidal choroidal vasculopathy
CUI: C1504336
Disease: Polypoidal choroidal vasculopathy
67 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 0.010 1.000 1 2018 2018