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: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		Cardiovascular Diseases 0.010 1.000 1 2002 2002
dbSNP: rs1801253
rs1801253 		0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		Mental Disorders 0.010 1.000 1 2003 2003
dbSNP: rs1801252
rs1801252 		0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2005 2005
dbSNP: rs1801252
rs1801252 		0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		Cardiovascular Diseases 0.010 1.000 1 2005 2005
dbSNP: rs1801253
rs1801253 		0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		Cardiovascular Diseases 0.010 1.000 1 2005 2005
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: rs1801253
rs1801253 		0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0152136
Disease: Low Tension Glaucoma
Low Tension Glaucoma 		Eye Diseases 0.010 1.000 1 2006 2006
dbSNP: rs1801252
rs1801252 		0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2008 2008
dbSNP: rs1801253
rs1801253 		0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0085612
Disease: Ventricular arrhythmia
Ventricular arrhythmia 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2008 2008
dbSNP: rs1801252
rs1801252 		0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17
CUI: C1536220
Disease: ST segment elevation myocardial infarction
ST segment elevation myocardial infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2009 2009
dbSNP: rs1801253
rs1801253 		0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C1536220
Disease: ST segment elevation myocardial infarction
ST segment elevation myocardial infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2009 2009
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: C2919365
Disease: Macroalbuminuric diabetic nephropathy
Macroalbuminuric diabetic nephropathy 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.010 1.000 1 2010 2010
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: 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: 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: 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: rs1801252
rs1801252 		0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17
CUI: C0030193
Disease: Pain
Pain 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2013 2013
dbSNP: rs1801253
rs1801253 		0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0030193
Disease: Pain
Pain 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2013 2013
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: 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: 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: 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: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.020 1.000 2 2009 2014
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