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: 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
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: 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
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: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy
Pathological Conditions, Signs and Symptoms; 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: 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: 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: 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: 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: C0152136
Disease: Low Tension Glaucoma
Low Tension Glaucoma
Eye Diseases 0.010 1.000 1 2006 2006
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: rs1801253
rs1801253
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69
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: 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: 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: 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: 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: C0018572
Disease: Hand, Foot and Mouth Disease
Hand, Foot and Mouth Disease
Infections 0.010 < 0.001 1 2017 2017
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: 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: 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: C0020651
Disease: Hypotension, Orthostatic
Hypotension, Orthostatic
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2014 2014