Disease: Coronary heart disease
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8