rs11057830, SCARB1

N. diseases: 5
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.
Vitamin E Assay
CUI: C1142098
Disease: Vitamin E Assay
4 0.851 0.040 12 124822507 intron variant G/A snv 0.15 0.800 1.000 1 2011 2011
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.851 0.040 12 124822507 intron variant G/A snv 0.15 0.710 1.000 3 2017 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.851 0.040 12 124822507 intron variant G/A snv 0.15 0.710 1.000 2 2017 2019
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.851 0.040 12 124822507 intron variant G/A snv 0.15 0.700 1.000 1 2017 2017
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.851 0.040 12 124822507 intron variant G/A snv 0.15 0.010 1.000 1 2019 2019