rs9349379, PHACTR1

N. diseases: 19
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 heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.820 1.000 6 2011 2019
Common Migraine
CUI: C0338480
Disease: Common Migraine
62 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.810 1.000 3 2013 2016
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.800 1.000 4 2012 2016
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.800 1.000 2 2011 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.760 1.000 11 2015 2019
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.710 1.000 2 2011 2015
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.700 1.000 3 2016 2019
Headache
CUI: C0018681
Disease: Headache
75 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.700 1.000 1 2018 2018
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.020 1.000 2 2016 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.020 1.000 2 2018 2019
Aneurysm, Dissecting
CUI: C0002949
Disease: Aneurysm, Dissecting
4 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.010 1.000 1 2016 2016
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.010 1.000 1 2019 2019
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.010 1.000 1 2018 2018
Coronary Stenosis
CUI: C0242231
Disease: Coronary Stenosis
20 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.010 1.000 1 2012 2012
Deficiency of butyryl-CoA dehydrogenase
CUI: C0342783
Disease: Deficiency of butyryl-CoA dehydrogenase
47 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.010 1.000 1 2019 2019
Fibromuscular Dysplasia
CUI: C0016052
Disease: Fibromuscular Dysplasia
3 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.010 1.000 1 2019 2019
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.010 1.000 1 2019 2019
Migraine with Aura
CUI: C0154723
Disease: Migraine with Aura
56 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.010 1.000 1 2015 2015
Premature coronary artery atherosclerosis
CUI: C1867743
Disease: Premature coronary artery atherosclerosis
43 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.010 1.000 1 2016 2016