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: rs11014166
rs11014166
0.882 0.040 10 18419869 intron variant A/T snv 0.27
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.710 1.000 2 2010 2011
dbSNP: rs61839258
rs61839258
0.882 0.040 10 18400709 5 prime UTR variant G/A;C;T snv 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2010 2010