rs6511720, LDLR

N. diseases: 15
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.
Low density lipoprotein cholesterol measurement
1142 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.800 1.000 17 2008 2019
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.700 1.000 10 2008 2013
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.800 1.000 7 2010 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.720 1.000 4 2011 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.710 1.000 3 2013 2018
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.810 1.000 2 2013 2017
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.800 1.000 1 2011 2011
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.700 1.000 1 2012 2012
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.010 1.000 1 2013 2013
Lipids measurement
CUI: C0523744
Disease: Lipids measurement
53 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.700 1.000 1 2009 2009
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.010 1.000 1 2009 2009
Pseudocholinesterase Measurement
CUI: C1168443
Disease: Pseudocholinesterase Measurement
568 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.700 1.000 1 2011 2011
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.700 1.000 1 2012 2012
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.700 1.000 1 2012 2012
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.700 1.000 1 2009 2009