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: rs9818870
rs9818870
0.878 0.036 3 138403280 3 prime UTR variant C/A,T snp 6.4E-05; 0.12
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.800 3 2009 2014
dbSNP: rs2306374
rs2306374
1.000 0.036 3 138401110 intron variant T/C snp 0.11
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.800 1 2011 2011