rs12526453, PHACTR1

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 0.827 0.160 6 12927312 intron variant C/G snv 0.27 0.730 1.000 4 2013 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.827 0.160 6 12927312 intron variant C/G snv 0.27 0.820 1.000 4 2011 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.827 0.160 6 12927312 intron variant C/G snv 0.27 0.820 1.000 3 2009 2015
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.827 0.160 6 12927312 intron variant C/G snv 0.27 0.010 1.000 1 2019 2019
Hyperlipoproteinemia Type IIa
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
661 0.827 0.160 6 12927312 intron variant C/G snv 0.27 0.010 1.000 1 2019 2019