rs7626962, SCN5A

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.
Sudden infant death syndrome
CUI: C0038644
Disease: Sudden infant death syndrome
68 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 0.750 0.800 5 2006 2011
Left ventricular noncompaction
CUI: C1960469
Disease: Left ventricular noncompaction
26 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 0.700 0
LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding)
CUI: C1838527
Disease: LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding)
1 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 0.700 0
Ventricular arrhythmia
CUI: C0085612
Disease: Ventricular arrhythmia
37 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 0.020 1.000 2 2002 2011
Acidosis, Respiratory
CUI: C0001127
Disease: Acidosis, Respiratory
1 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 0.010 1.000 1 2006 2006
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 0.010 1.000 1 2014 2014
Cardiac Arrhythmia
CUI: C0003811
Disease: Cardiac Arrhythmia
111 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 0.010 1.000 1 2011 2011
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 0.010 1.000 1 2011 2011
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 0.010 1.000 1 2011 2011
Syncope
CUI: C0039070
Disease: Syncope
45 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 0.010 1.000 1 2002 2002