rs10501920, CNTN5

N. diseases: 3
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 0.882 0.080 11 99622442 intron variant C/G snv 0.14 0.010 1.000 1 2007 2007
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.882 0.080 11 99622442 intron variant C/G snv 0.14 0.010 1.000 1 2007 2007
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.882 0.080 11 99622442 intron variant C/G snv 0.14 0.010 1.000 1 2007 2007