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.
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.010 1.000 1 2016 2016
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.700 1.000 3 2017 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.070 1.000 7 2001 2018
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
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
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.040 0.500 4 2002 2014
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
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
Body Height
CUI: C0005890
Disease: Body Height
3972 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 0.700 1.000 1 2019 2019