rs768963, CACTIN

N. diseases: 2
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.
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.925 0.120 19 3615409 non coding transcript exon variant G/A;C snv 0.030 1.000 3 2006 2015
Large-artery atherosclerosis (embolus/thrombosis)
CUI: C4699512
Disease: Large-artery atherosclerosis (embolus/thrombosis)
35 0.925 0.120 19 3615409 non coding transcript exon variant G/A;C snv 0.010 1.000 1 2013 2013