Disease: Coronary Artery 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
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs715
CPS1
1.000 0.040 2 210678331 3 prime UTR variant T/C snv 0.28 13
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 12
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 11
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
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