rs1042713, ADRB2

N. diseases: 63
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.
Signs and Symptoms, Respiratory
CUI: C0037090
Disease: Signs and Symptoms, Respiratory
10 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2011 2011
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.060 0.833 6 2010 2018
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2010 2010
End stage cardiac failure
CUI: C1868938
Disease: End stage cardiac failure
2 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2010 2010
High altitude pulmonary edema
CUI: C0340100
Disease: High altitude pulmonary edema
45 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2010 2010
Intermittent Claudication
CUI: C0021775
Disease: Intermittent Claudication
69 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2010 2010
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2010 2010
Pain
CUI: C0030193
Disease: Pain
196 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2010 2010
Allergic sensitization
CUI: C3662483
Disease: Allergic sensitization
26 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2009 2009
Juvenile arthritis
CUI: C3495559
Disease: Juvenile arthritis
128 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2009 2009
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2009 2009
ST segment elevation myocardial infarction
CUI: C1536220
Disease: ST segment elevation myocardial infarction
16 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2009 2009
Hypoglycemia
CUI: C0020615
Disease: Hypoglycemia
42 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.020 1.000 2 2008 2011
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2008 2008
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2008 2008
Loss of hypoglycemic warning
CUI: C0342317
Disease: Loss of hypoglycemic warning
1 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2008 2008
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.040 1.000 4 2007 2018
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.040 1.000 4 2007 2018
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2007 2007
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2007 2007
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2006 2006
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.030 0.667 3 2005 2013
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.030 1.000 3 2005 2010
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.020 0.500 2 2005 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.020 1.000 2 2005 2008