rs1801253, ADRB1

N. diseases: 34
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.
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2015 2015
Mood Disorders
CUI: C0525045
Disease: Mood Disorders
308 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2003 2003
Obesity
CUI: C0028754
Disease: Obesity
1111 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.030 0.667 3 2006 2018
Pain
CUI: C0030193
Disease: Pain
196 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2013 2013
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2015 2015
ST segment elevation myocardial infarction
CUI: C1536220
Disease: ST segment elevation myocardial infarction
16 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2009 2009
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.700 1.000 4 2016 2019
Thyrotoxicosis
CUI: C0040156
Disease: Thyrotoxicosis
7 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2014 2014
Ventricular arrhythmia
CUI: C0085612
Disease: Ventricular arrhythmia
37 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2008 2008