ADRB1, adrenoceptor beta 1, 153

N. diseases: 130; N. variants: 3
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1801253
rs1801253
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
Cardiovascular Diseases 0.100 0.929 14 2003 2019
dbSNP: rs1801253
rs1801253
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0018801
Disease: Heart failure
Heart failure
Cardiovascular Diseases 0.100 0.917 12 2003 2019
dbSNP: rs1801253
rs1801253
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.070 1.000 7 2001 2018
dbSNP: rs1801252
rs1801252
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17
CUI: C0018801
Disease: Heart failure
Heart failure
Cardiovascular Diseases 0.060 1.000 6 2000 2019
dbSNP: rs1801252
rs1801252
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
Cardiovascular Diseases 0.060 1.000 6 2000 2019
dbSNP: rs1801253
rs1801253
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
Cardiovascular Diseases 0.060 0.833 6 2008 2018
dbSNP: rs1801253
rs1801253
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
Cardiovascular Diseases 0.740 1.000 5 2006 2019
dbSNP: rs1801253
rs1801253
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.040 0.500 4 2002 2014
dbSNP: rs1801253
rs1801253
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 4 2016 2019
dbSNP: rs1801252
rs1801252
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
Cardiovascular Diseases 0.030 0.667 3 2009 2018
dbSNP: rs1801252
rs1801252
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.030 0.667 3 2001 2013
dbSNP: rs1801252
rs1801252
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.030 1.000 3 2010 2014
dbSNP: rs1801253
rs1801253
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 3 2017 2018
dbSNP: rs1801253
rs1801253
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.030 1.000 3 2012 2014
dbSNP: rs1801253
rs1801253
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.030 0.667 3 2006 2018
dbSNP: rs1801253
rs1801253
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.030 1.000 3 2008 2014
dbSNP: rs1801252
rs1801252
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
Cardiovascular Diseases 0.020 1.000 2 2012 2012
dbSNP: rs1801252
rs1801252
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.020 1.000 2 2002 2006
dbSNP: rs1801252
rs1801252
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
Cardiovascular Diseases 0.020 1.000 2 2009 2014
dbSNP: rs1801253
rs1801253
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0264716
Disease: Chronic heart failure
Chronic heart failure
Cardiovascular Diseases 0.020 1.000 2 2011 2013
dbSNP: rs1801253
rs1801253
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
Cardiovascular Diseases 0.020 1.000 2 2002 2012
dbSNP: rs1801253
rs1801253
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.020 1.000 2 2003 2010
dbSNP: rs1801253
rs1801253
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0005612
Disease: Birth Weight
Birth Weight
Pathological Conditions, Signs and Symptoms 0.800 1.000 2 2013 2019
dbSNP: rs1801253
rs1801253
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases 0.020 1.000 2 2005 2016
dbSNP: rs1203958828
rs1203958828
1.000 0.040 10 114044322 synonymous variant C/T snv 1.4E-05
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2014 2014