rs10846744, SCARB1

N. diseases: 11
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.
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.763 0.160 12 124827879 intron variant G/C snv 0.32 0.700 1.000 1 2018 2018
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.763 0.160 12 124827879 intron variant G/C snv 0.32 0.040 0.750 4 2010 2018
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.763 0.160 12 124827879 intron variant G/C snv 0.32 0.040 0.750 4 2010 2018
Multiple Chronic Conditions
CUI: C3266262
Disease: Multiple Chronic Conditions
42 0.763 0.160 12 124827879 intron variant G/C snv 0.32 0.030 1.000 3 2010 2018
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.763 0.160 12 124827879 intron variant G/C snv 0.32 0.020 0.500 2 2012 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.763 0.160 12 124827879 intron variant G/C snv 0.32 0.020 1.000 2 2017 2018
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.763 0.160 12 124827879 intron variant G/C snv 0.32 0.020 1.000 2 2012 2018
Pseudohyperkalemia Cardiff
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
60 0.763 0.160 12 124827879 intron variant G/C snv 0.32 0.020 1.000 2 2016 2017
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.763 0.160 12 124827879 intron variant G/C snv 0.32 0.010 1.000 1 2017 2017
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.763 0.160 12 124827879 intron variant G/C snv 0.32 0.010 1.000 1 2018 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.763 0.160 12 124827879 intron variant G/C snv 0.32 0.010 1.000 1 2018 2018