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
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 4
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 4