rs1466535, LRP1

N. diseases: 9
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.
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.790 0.160 12 57140687 intron variant G/A;C snv 0.840 1.000 4 2011 2015
Apraxia, Developmental Verbal
CUI: C0750927
Disease: Apraxia, Developmental Verbal
21 0.790 0.160 12 57140687 intron variant G/A;C snv 0.010 1 2014 2014
Arteriovenous fistula
CUI: C0003855
Disease: Arteriovenous fistula
8 0.790 0.160 12 57140687 intron variant G/A;C snv 0.010 1.000 1 2013 2013
Carotid Artery Diseases
CUI: C0007273
Disease: Carotid Artery Diseases
6 0.790 0.160 12 57140687 intron variant G/A;C snv 0.010 1.000 1 2014 2014
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.790 0.160 12 57140687 intron variant G/A;C snv 0.010 1.000 1 2014 2014
Carotid Stenosis
CUI: C0007282
Disease: Carotid Stenosis
19 0.790 0.160 12 57140687 intron variant G/A;C snv 0.010 1.000 1 2014 2014
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.790 0.160 12 57140687 intron variant G/A;C snv 0.010 1.000 1 2011 2011
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.790 0.160 12 57140687 intron variant G/A;C snv 0.010 1.000 1 2011 2011
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.790 0.160 12 57140687 intron variant G/A;C snv 0.010 1.000 1 2011 2011