rs1860561, ATP2A2

N. diseases: 5
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
CUI: C0004238
Disease: Atrial Fibrillation
584 0.851 0.080 12 110345436 intron variant G/A snv 0.19 0.010 1.000 1 2013 2013
Cardiac Arrhythmia
CUI: C0003811
Disease: Cardiac Arrhythmia
111 0.851 0.080 12 110345436 intron variant G/A snv 0.19 0.010 1.000 1 2013 2013
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.851 0.080 12 110345436 intron variant G/A snv 0.19 0.010 1.000 1 2013 2013
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.851 0.080 12 110345436 intron variant G/A snv 0.19 0.010 1.000 1 2013 2013
Ventricular arrhythmia
CUI: C0085612
Disease: Ventricular arrhythmia
37 0.851 0.080 12 110345436 intron variant G/A snv 0.19 0.010 1.000 1 2013 2013