Disease: Coronary heart disease
Source: ALL
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 62
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs139401390 0.851 0.120 10 88643382 regulatory region variant A/G snv 1.0E-02 5
rs116092985
PKD1
0.882 0.040 16 2110972 missense variant A/G snv 6.5E-02 7.8E-02 4