rs2048327, SLC22A3

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.
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.851 0.120 6 160442500 intron variant T/C snv 0.28 0.700 1.000 3 2009 2014
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.851 0.120 6 160442500 intron variant T/C snv 0.28 0.700 1.000 2 2009 2014
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.851 0.120 6 160442500 intron variant T/C snv 0.28 0.010 1.000 1 2019 2019
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.851 0.120 6 160442500 intron variant T/C snv 0.28 0.010 1.000 1 2019 2019
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.851 0.120 6 160442500 intron variant T/C snv 0.28 0.010 1.000 1 2019 2019