Disease: Coronary Artery Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs2246942
LIPA
0.925 0.040 10 89245129 intron variant A/C;G snv 2
rs2254638
N6AMT1
0.882 0.040 21 28883961 intron variant A/C;G snv 3
rs2267788
LOC105371077 ; GRIN2A
0.882 0.040 16 9794742 intron variant C/T snv 3
rs2281727
SMG6
0.882 0.080 17 2214651 intron variant A/G snv 0.38 4
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2306374
MRAS
0.925 0.040 3 138401110 intron variant T/C snv 0.12 2
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs2430561
IFNG ; IFNG-AS1
0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 10
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6
rs2505083
JCAD
0.882 0.080 10 30046193 intron variant T/C snv 0.33 3
rs255052
DPEP2 ; DUS2
0.925 0.040 16 67991092 intron variant G/A snv 0.17 0.17 4
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14 6
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 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
rs2891168
CDKN2B-AS1
0.851 0.160 9 22098620 intron variant A/G snv 0.40 5
rs2895811
HHIPL1
0.851 0.080 14 99667605 intron variant T/A;C snv 4
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs3127599
LPAL2
0.925 0.040 6 160486102 intron variant C/T snv 0.28 2
rs321159
MYO1D
0.882 0.040 17 32628611 intron variant A/G;T snv 3
rs342293
CTB-30L5.1
0.882 0.040 7 106731773 intron variant C/G snv 0.42 7