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: rs1187513719
rs1187513719
0.851 0.200 10 94780595 missense variant A/G snv 4.0E-06
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs4244285
rs4244285
0.695 0.360 10 94781859 synonymous variant G/A;C snv 0.18
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2010 2010