rs16847548, None

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.
QT interval feature (observable entity)
CUI: C0429028
Disease: QT interval feature (observable entity)
226 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 0.700 1.000 2 2009 2012
Cardiac Arrest
CUI: C0018790
Disease: Cardiac Arrest
50 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 0.010 1.000 1 2019 2019
cardiac event
CUI: C0741923
Disease: cardiac event
18 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 0.010 1.000 1 2010 2010
Congenital long QT syndrome
CUI: C1141890
Disease: Congenital long QT syndrome
54 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 0.010 1 2013 2013
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 0.010 1 2009 2009
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 0.010 1 2009 2009
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 0.010 1 2009 2009
Long QT Syndrome
CUI: C0023976
Disease: Long QT Syndrome
349 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 0.010 1.000 1 2019 2019