Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12526453
rs12526453
0.827 0.160 6 12927312 intron variant C/G snv 0.27
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.820 1.000 3 2009 2015
dbSNP: rs9349379
rs9349379
0.732 0.200 6 12903725 intron variant A/G snv 0.32
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.710 1.000 2 2011 2015
dbSNP: rs9369640
rs9369640
0.851 0.080 6 12901209 intron variant C/A;G snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2015 2015