Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
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
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 8
rs11513729 1.000 0.080 12 111835695 downstream gene variant C/T snv 0.29 5
rs7395662 0.882 0.080 11 48497341 downstream gene variant A/G snv 0.56 5
rs852426
ACTB
0.882 0.240 7 5526722 downstream gene variant C/T snv 0.39 5
rs10937273 0.882 0.160 3 186831906 downstream gene variant G/A snv 0.33 4
rs12425791 0.882 0.120 12 674318 downstream gene variant G/A;C snv 4
rs2005108 1.000 0.080 11 102899623 downstream gene variant C/G;T snv 3
rs6825454 1.000 0.080 4 154580036 downstream gene variant T/C snv 0.25 3
rs231150
TRPS1
0.925 0.080 8 115408099 downstream gene variant A/T snv 0.55 2
rs3917639 0.925 0.120 1 94527220 downstream gene variant C/T snv 2
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs689466
PACERR ; PTGS2
0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28