Source: GWASDB

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: rs2891168
rs2891168
0.851 0.160 9 22098620 intron variant A/G snv 0.40
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.820 1.000 1 2007 2018
dbSNP: rs2891168
rs2891168
0.851 0.160 9 22098620 intron variant A/G snv 0.40
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 3 2011 2013
dbSNP: rs2891168
rs2891168
0.851 0.160 9 22098620 intron variant A/G snv 0.40
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013