rs1800888, ADRB2

N. diseases: 23
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.
Asthma
CUI: C0004096
Disease: Asthma
1536 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.060 1.000 6 2006 2019
Bronchiolitis
CUI: C0006271
Disease: Bronchiolitis
32 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1.000 1 2015 2015
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1.000 1 2012 2012
Childhood asthma
CUI: C0264408
Disease: Childhood asthma
317 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1.000 1 2013 2013
Chronic heart failure
CUI: C0264716
Disease: Chronic heart failure
11 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1.000 1 2006 2006
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.030 1.000 3 2012 2016
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.040 1.000 4 2001 2010
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1.000 1 2019 2019
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1.000 1 2012 2012
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1.000 1 2012 2012
Forced expiratory volume function
CUI: C0016529
Disease: Forced expiratory volume function
1169 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.700 1.000 2 2017 2019
Glaucoma, Primary Open Angle
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
222 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1 2003 2003
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.020 1.000 2 2009 2010
HETEROTAXY, VISCERAL, 2, AUTOSOMAL
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
5 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1.000 1 2006 2006
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1.000 1 2012 2012
Left Ventricular Hypertrophy
CUI: C0149721
Disease: Left Ventricular Hypertrophy
67 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1.000 1 2006 2006
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1.000 1 2009 2009
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1.000 1 2006 2006
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1.000 1 2012 2012
Obesity
CUI: C0028754
Disease: Obesity
1111 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1 2012 2012
peak expiratory flow (procedure)
CUI: C1518922
Disease: peak expiratory flow (procedure)
119 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.700 1.000 1 2019 2019
Primary congenital glaucoma
CUI: C1533041
Disease: Primary congenital glaucoma
25 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1 2003 2003
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
14 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1.000 1 2015 2015