Disease: Coronary Artery Disease
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 8
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 8
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14 4