rs699, AGT

N. diseases: 134
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 neoplasm of colon and/or rectum
502 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2020 2020
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
138 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2019 2019
Muscle damage
CUI: C0410158
Disease: Muscle damage
4 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2019 2019
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.700 1.000 1 2019 2019
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
24 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2017 2017
Erythrocytosis due to low atmospheric pressure
13 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2017 2017
Metabolic Diseases
CUI: C0025517
Disease: Metabolic Diseases
50 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2017 2017
Mean blood pressure
CUI: C0428886
Disease: Mean blood pressure
344 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.700 1.000 1 2016 2016
Dystrophia myotonica 2
CUI: C2931689
Disease: Dystrophia myotonica 2
21 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2015 2015
Henoch-Schonlein purpura nephritis
CUI: C2721603
Disease: Henoch-Schonlein purpura nephritis
6 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2015 2015
Hyperaldosteronism
CUI: C0020428
Disease: Hyperaldosteronism
6 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2015 2015
Left ventricular systolic dysfunction
11 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2015 2015
Renal cyst
CUI: C3887499
Disease: Renal cyst
17 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2015 2015
Chronic glomerulonephritis
CUI: C0152451
Disease: Chronic glomerulonephritis
7 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2014 2014
Prehypertension
CUI: C1696708
Disease: Prehypertension
5 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2014 2014
Brain Infarction
CUI: C0751955
Disease: Brain Infarction
11 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2013 2013
Ovarian Failure, Premature
CUI: C0085215
Disease: Ovarian Failure, Premature
115 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2013 2013
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 1.000 2 2012 2020
Acute myocardial infarction
CUI: C0155626
Disease: Acute myocardial infarction
118 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.040 0.750 4 2011 2018
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
635 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.030 1.000 3 2011 2017
Acromegaly
CUI: C0001206
Disease: Acromegaly
25 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 1.000 2 2011 2017
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 1.000 2 2011 2011
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 1.000 2 2011 2011
ST segment elevation myocardial infarction
16 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.020 1.000 2 2011 2012
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
220 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.700 1.000 1 2011 2011