Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10797432
LOC100996583
1.000 0.040 1 2569899 downstream gene variant C/T snv 0.51 2
rs1518108 0.925 0.080 1 206869829 downstream gene variant C/T snv 0.47 2
rs2108225 1.000 0.040 7 107812658 downstream gene variant G/A;T snv 2
rs2542152 0.925 0.040 18 12782762 downstream gene variant T/C;G snv 2
rs4676408 1.000 0.040 2 240634984 downstream gene variant G/A;T snv 0.57 2
rs10910092
LOC100996583
1.000 0.040 1 2570077 downstream gene variant A/G snv 0.52 1
rs11083840
PTGIR
1.000 0.040 19 46616653 downstream gene variant T/G snv 0.44 1
rs17771967 1.000 0.040 19 54868759 downstream gene variant A/G snv 0.42 1
rs4720672
RAC1
1.000 0.040 7 6404208 downstream gene variant T/C snv 0.14 1
rs7210086
SLC39A11 ; LOC105371887
1.000 0.040 17 72645559 downstream gene variant A/C snv 0.17 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs689466
PACERR ; PTGS2
0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs4796793
STAT3
0.716 0.320 17 42390192 upstream gene variant G/C snv 0.67 16
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13