rs2781666, ARG1

N. diseases: 8
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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.790 0.280 6 131572419 intron variant G/T snv 0.45 0.020 1.000 2 2014 2018
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.790 0.280 6 131572419 intron variant G/T snv 0.45 0.020 1.000 2 2007 2010
Asthma
CUI: C0004096
Disease: Asthma
1536 0.790 0.280 6 131572419 intron variant G/T snv 0.45 0.010 1.000 1 2018 2018
Bronchopulmonary Dysplasia
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
112 0.790 0.280 6 131572419 intron variant G/T snv 0.45 0.010 1.000 1 2014 2014
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.790 0.280 6 131572419 intron variant G/T snv 0.45 0.010 1.000 1 2019 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.790 0.280 6 131572419 intron variant G/T snv 0.45 0.010 1.000 1 2019 2019
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.790 0.280 6 131572419 intron variant G/T snv 0.45 0.010 1.000 1 2018 2018
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.790 0.280 6 131572419 intron variant G/T snv 0.45 0.010 1.000 1 2018 2018