rs10033464, None

N. diseases: 8
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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 0.010 1 2012 2012
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 0.030 0.667 3 2008 2016
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 0.900 0.933 15 2007 2019
Cardioembolic stroke
CUI: C1531624
Disease: Cardioembolic stroke
28 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 0.010 1.000 1 2013 2013
Cat eye syndrome
CUI: C0265493
Disease: Cat eye syndrome
6 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 0.010 1.000 1 2008 2008
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 0.010 1.000 1 2013 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 0.010 1.000 1 2017 2017
Paroxysmal atrial fibrillation
CUI: C0235480
Disease: Paroxysmal atrial fibrillation
8 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 0.010 1.000 1 2019 2019