rs769665945, SERPINE1

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.
Dementia, Vascular
CUI: C0011269
Disease: Dementia, Vascular
32 0.882 0.160 7 101137079 missense variant C/A;T snv 4.0E-06; 3.6E-05 0.010 1 2006 2006
First myocardial infarction
CUI: C1273976
Disease: First myocardial infarction
7 0.882 0.160 7 101137079 missense variant C/A;T snv 4.0E-06; 3.6E-05 0.010 1.000 1 2014 2014
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.882 0.160 7 101137079 missense variant C/A;T snv 4.0E-06; 3.6E-05 0.010 1.000 1 2014 2014