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.
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
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
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.700 1.000 4 2016 2019
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.700 1.000 3 2017 2018
Body Height
CUI: C0005890
Disease: Body Height
3972 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.700 1.000 1 2019 2019
Diastolic blood pressure measurement
CUI: C1305849
Disease: 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
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
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
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.070 1.000 7 2001 2018
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
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.040 0.500 4 2002 2014
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
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
Obesity
CUI: C0028754
Disease: Obesity
1111 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.030 0.667 3 2006 2018
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 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
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
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
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
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
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
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2016 2016
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
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