rs3745297, HRC

N. diseases: 10
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.
Paroxysmal atrial fibrillation
CUI: C0235480
Disease: Paroxysmal atrial fibrillation
8 0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 0.010 1.000 1 2019 2019
Ventricular arrhythmia
CUI: C0085612
Disease: Ventricular arrhythmia
37 0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 0.050 1.000 5 2008 2017
Cardiac Arrhythmia
CUI: C0003811
Disease: Cardiac Arrhythmia
111 0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 0.040 1.000 4 2011 2018
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 0.020 1.000 2 2011 2018
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 0.020 1.000 2 2011 2018
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 0.030 1.000 3 2008 2017
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 0.010 1.000 1 2019 2019
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 0.010 1.000 1 2019 2019
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 0.010 1.000 1 2019 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 0.010 1.000 1 2019 2019