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
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs460976 0.851 0.120 21 41463567 downstream gene variant A/G;T snv 7
rs852426
ACTB
0.882 0.240 7 5526722 downstream gene variant C/T snv 0.39 5
rs12425791 0.882 0.120 12 674318 downstream gene variant G/A;C snv 4
rs11750568 1.000 0.080 5 179108712 downstream gene variant A/G;T snv 3
rs2005108 1.000 0.080 11 102899623 downstream gene variant C/G;T snv 3
rs2219939 1.000 0.040 15 78737381 downstream gene variant G/A snv 0.53 3
rs6825454 1.000 0.080 4 154580036 downstream gene variant T/C snv 0.25 3
rs230119 1.000 0.080 9 119152945 downstream gene variant C/A;T snv 2
rs3851059 10 80270902 downstream gene variant G/A snv 0.27 2
rs11681884 2 113090051 downstream gene variant C/T snv 0.21 1
rs2815063 6 39294759 downstream gene variant C/A snv 0.22 1
rs4867766
LOC105377739
5 174535039 downstream gene variant G/A snv 0.17 1
rs731991 22 30629202 downstream gene variant A/G;T snv 1
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22