Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs4646903
CYP1A1
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs3027898
IRAK1
0.752 0.360 X 154010439 downstream gene variant C/A snv 11
rs61776719 0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46 11
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 10
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 10
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 8
rs112635299
SERPINA2
1.000 0.040 14 94371805 downstream gene variant G/T snv 1.3E-02 7
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv 7
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs7395662 0.882 0.080 11 48497341 downstream gene variant A/G snv 0.56 5
rs1870634 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 4
rs198388
NPPB
0.851 0.160 1 11857283 downstream gene variant C/G;T snv 4
rs2768759 0.851 0.200 1 156882671 downstream gene variant A/C;G snv 4
rs2967605
RAB11B
0.925 0.040 19 8404854 downstream gene variant C/T snv 0.20 4
rs3931020 0.882 0.040 1 74769633 downstream gene variant T/C snv 0.71 4
rs2814944 1.000 0.040 6 34585020 downstream gene variant G/A snv 0.20 3
rs614230
CX3CL1
1.000 0.040 16 57385374 downstream gene variant C/T snv 0.61 2
rs659418
SERPINH1
1.000 0.040 11 75573289 downstream gene variant T/G snv 0.19 2