rs711752, 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.
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 1.000 0.040 16 56962299 splice region variant G/A;C snv 0.800 1.000 4 2008 2016
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 1.000 0.040 16 56962299 splice region variant G/A;C snv 0.700 1.000 3 2008 2013
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
624 1.000 0.040 16 56962299 splice region variant G/A;C snv 0.700 1.000 1 2016 2016
Pseudocholinesterase Measurement
CUI: C1168443
Disease: Pseudocholinesterase Measurement
568 1.000 0.040 16 56962299 splice region variant G/A;C snv 0.700 1.000 1 2011 2011
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 1.000 0.040 16 56962299 splice region variant G/A;C snv 0.700 1.000 1 2012 2012
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 1.000 0.040 16 56962299 splice region variant G/A;C snv 0.700 1.000 1 2012 2012
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 1.000 0.040 16 56962299 splice region variant G/A;C snv 0.700 1.000 1 2009 2009
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 1.000 0.040 16 56962299 splice region variant G/A;C snv 0.010 1.000 1 2015 2015
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1.000 0.040 16 56962299 splice region variant G/A;C snv 0.010 1.000 1 2017 2017
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 1.000 0.040 16 56962299 splice region variant G/A;C snv 0.010 1.000 1 2017 2017