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: 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: 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: 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: 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: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.030 1.000 3 2012 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: 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: 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: 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
dbSNP: rs1801252
rs1801252 		0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17
CUI: C0040156
Disease: Thyrotoxicosis
Thyrotoxicosis 		Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1801252
rs1801252 		0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1801253
rs1801253 		0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0040156
Disease: Thyrotoxicosis
Thyrotoxicosis 		Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1801253
rs1801253 		0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0020651
Disease: Hypotension, Orthostatic
Hypotension, Orthostatic 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1801252
rs1801252 		0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1801253
rs1801253 		0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs1801253
rs1801253 		0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2015 2015
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: rs1801253
rs1801253 		0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1801253
rs1801253 		0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0242231
Disease: Coronary Stenosis
Coronary Stenosis 		Cardiovascular Diseases 0.010 1.000 1 2016 2016
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: rs1801252
rs1801252 		0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17
CUI: C0027765
Disease: nervous system disorder
nervous system disorder 		Nervous System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1801253
rs1801253 		0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0014378
Disease: Enterovirus Infections
Enterovirus Infections 		Infections 0.010 1.000 1 2017 2017
dbSNP: rs1801253
rs1801253 		0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
CUI: C0018572
Disease: Hand, Foot and Mouth Disease
Hand, Foot and Mouth Disease 		Infections 0.010 < 0.001 1 2017 2017