rs499818, None

N. diseases: 4
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.851 0.080 6 13332235 upstream gene variant G/A snv 0.21 0.020 1.000 2 2007 2011
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.851 0.080 6 13332235 upstream gene variant G/A snv 0.21 0.010 1.000 1 2007 2007
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.851 0.080 6 13332235 upstream gene variant G/A snv 0.21 0.010 1.000 1 2007 2007
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.851 0.080 6 13332235 upstream gene variant G/A snv 0.21 0.010 1.000 1 2007 2007