rs1801253, ADRB1

N. diseases: 34
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.
Macroalbuminuric diabetic nephropathy
2 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2010 2010
Thyrotoxicosis
CUI: C0040156
Disease: Thyrotoxicosis
7 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2014 2014
Chronic heart failure
CUI: C0264716
Disease: Chronic heart failure
11 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.020 1.000 2 2011 2013
Enterovirus Infections
CUI: C0014378
Disease: Enterovirus Infections
12 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2017 2017
Hand, Foot and Mouth Disease
CUI: C0018572
Disease: Hand, Foot and Mouth Disease
13 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1 2017 2017
ST segment elevation myocardial infarction
16 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2009 2009
Coronary Stenosis
CUI: C0242231
Disease: Coronary Stenosis
20 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2016 2016
Hypotension, Orthostatic
CUI: C0020651
Disease: Hypotension, Orthostatic
21 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2014 2014
Ventricular arrhythmia
CUI: C0085612
Disease: Ventricular arrhythmia
37 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2008 2008
Low Tension Glaucoma
CUI: C0152136
Disease: Low Tension Glaucoma
56 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2006 2006
Left Ventricular Hypertrophy
CUI: C0149721
Disease: Left Ventricular Hypertrophy
67 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.030 1.000 3 2008 2014
Diastolic blood pressure measurement
81 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.700 1.000 1 2018 2018
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.020 1.000 2 2003 2010
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.020 1.000 2 2005 2016
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2005 2005
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.100 0.929 14 2003 2019
Pain
CUI: C0030193
Disease: Pain
196 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2013 2013
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.100 0.917 12 2003 2019
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.020 1.000 2 2002 2012
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.060 0.833 6 2008 2018
Mood Disorders
CUI: C0525045
Disease: Mood Disorders
308 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2003 2003
Birth Weight
CUI: C0005612
Disease: Birth Weight
369 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.800 1.000 2 2013 2019
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2002 2002
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.030 1.000 3 2012 2014
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.740 1.000 5 2006 2019