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: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.720 1.000 2 2003 2004
dbSNP: rs12316150
rs12316150
1.000 0.080 12 10159692 3 prime UTR variant A/T snv 7.4E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 0