Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2069840
rs2069840
0.742 0.360 7 22728953 intron variant C/G snv 0.27
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.010 1.000 1 2008 2008