Disease: Coronary Arteriosclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs4888378
CFDP1
0.851 0.040 16 75298143 intron variant A/G snv 0.52 4
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4673
CYBA
0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs4149313
ABCA1
0.763 0.240 9 104824472 missense variant T/C snv 9
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs3900940
MYH15
0.827 0.040 3 108428881 missense variant T/A;C snv 4.3E-06; 0.24 6
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs375752214
NOS3
0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 22
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs3732379
CX3CR1
0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs267606661
APOE
0.763 0.120 19 44909101 missense variant C/G;T snv 3.9E-04; 1.0E-05 10
rs2518136
AHSG
0.851 0.120 3 186620038 intron variant T/C snv 0.46 4
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6