rs120074192, KCNQ1

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.
Atrial Fibrillation, Familial, 3
CUI: C1837014
Disease: Atrial Fibrillation, Familial, 3
10 0.763 0.120 11 2527959 missense variant A/G snv 0.800 1.000 1 2003 2003
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.763 0.120 11 2527959 missense variant A/G snv 0.050 1.000 5 2003 2018
Cardiac Arrhythmia
CUI: C0003811
Disease: Cardiac Arrhythmia
111 0.763 0.120 11 2527959 missense variant A/G snv 0.030 1.000 3 2007 2014
Long QT Syndrome
CUI: C0023976
Disease: Long QT Syndrome
349 0.763 0.120 11 2527959 missense variant A/G snv 0.020 1.000 2 2003 2004
Atrioventricular Block
CUI: C0004245
Disease: Atrioventricular Block
17 0.763 0.120 11 2527959 missense variant A/G snv 0.010 1.000 1 2007 2007
Cardiac Arrest
CUI: C0018790
Disease: Cardiac Arrest
50 0.763 0.120 11 2527959 missense variant A/G snv 0.010 1.000 1 2018 2018
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.763 0.120 11 2527959 missense variant A/G snv 0.010 1.000 1 2007 2007
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.763 0.120 11 2527959 missense variant A/G snv 0.010 1 2007 2007
Multiple Chronic Conditions
CUI: C3266262
Disease: Multiple Chronic Conditions
42 0.763 0.120 11 2527959 missense variant A/G snv 0.010 1.000 1 2018 2018
Ventricular arrhythmia
CUI: C0085612
Disease: Ventricular arrhythmia
37 0.763 0.120 11 2527959 missense variant A/G snv 0.010 1.000 1 2018 2018