rs4783961, CETP

N. diseases: 7
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 0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47 0.800 1.000 4 2012 2019
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47 0.700 1.000 3 2012 2012
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47 0.700 1.000 1 2012 2012
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47 0.010 1.000 1 2018 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47 0.010 1.000 1 2018 2018
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47 0.010 1.000 1 2019 2019
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47 0.010 1.000 1 2019 2019