rs2026458, PHACTR1

N. diseases: 6
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.
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 0.882 0.080 6 12825642 intron variant C/T snv 0.34 0.700 1.000 1 2011 2011
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.882 0.080 6 12825642 intron variant C/T snv 0.34 0.020 1.000 2 2016 2019
Carotid artery calcification
CUI: C4285890
Disease: Carotid artery calcification
3 0.882 0.080 6 12825642 intron variant C/T snv 0.34 0.010 1.000 1 2015 2015
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.882 0.080 6 12825642 intron variant C/T snv 0.34 0.010 1.000 1 2019 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.882 0.080 6 12825642 intron variant C/T snv 0.34 0.010 1.000 1 2016 2016
Premature coronary artery atherosclerosis
CUI: C1867743
Disease: Premature coronary artery atherosclerosis
43 0.882 0.080 6 12825642 intron variant C/T snv 0.34 0.010 1.000 1 2016 2016