rs1864163, CETP

N. diseases: 10
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.
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.882 0.120 16 56963321 intron variant G/A snv 0.26 0.810 1.000 2 2013 2019
High density lipoprotein measurement
1440 0.882 0.120 16 56963321 intron variant G/A snv 0.26 0.800 1.000 5 2008 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.882 0.120 16 56963321 intron variant G/A snv 0.26 0.800 1.000 3 2012 2019
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.882 0.120 16 56963321 intron variant G/A snv 0.26 0.700 1.000 3 2008 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.882 0.120 16 56963321 intron variant G/A snv 0.26 0.700 1.000 1 2011 2011
Lipids measurement
CUI: C0523744
Disease: Lipids measurement
53 0.882 0.120 16 56963321 intron variant G/A snv 0.26 0.700 1.000 1 2009 2009
Pseudocholinesterase Measurement
CUI: C1168443
Disease: Pseudocholinesterase Measurement
568 0.882 0.120 16 56963321 intron variant G/A snv 0.26 0.700 1.000 1 2011 2011
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.882 0.120 16 56963321 intron variant G/A snv 0.26 0.700 1.000 1 2012 2012
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.882 0.120 16 56963321 intron variant G/A snv 0.26 0.700 1.000 1 2009 2009
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.882 0.120 16 56963321 intron variant G/A snv 0.26 0.010 1.000 1 2018 2018