Disease: Coronary Artery Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 10
rs11024074
PLEKHA7
0.925 0.040 11 16895672 intron variant T/C snv 0.29 5
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 8
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 9
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 12
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv 8
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 15
rs7209400
LOC102724596
1.000 0.040 17 49372695 intron variant C/T snv 0.47 6
rs7500448
CDH13
1.000 0.040 16 83012185 intron variant A/G snv 0.20 3
rs7692387
GUCY1A1
0.925 0.080 4 155714157 intron variant G/A snv 0.16 5
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 9