Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs7025417
LOC107987046 ; IL33
0.752 0.280 9 6240084 intron variant T/C;G snv 11
rs1343151
IL23R
0.752 0.400 1 67253446 intron variant G/A snv 0.41 10
rs1417938
CRP
0.776 0.320 1 159714396 intron variant T/A;C snv 0.28 10
rs3838646
TTTY14
0.827 0.320 Y 18991182 intron variant CA/- del 8
rs6910071
TSBP1 ; TSBP1-AS1
0.790 0.320 6 32315077 intron variant A/G snv 0.14 7
rs17435
MECP2
0.851 0.200 X 154046529 intron variant T/A;C snv 4
rs3790567
IL12RB2
0.851 0.240 1 67356694 intron variant A/G snv 0.61 4
rs540386
TRAF6
0.851 0.200 11 36503743 intron variant C/G;T snv 4
rs128738
P4HA2
0.925 0.160 5 132205182 intron variant G/T snv 0.18 2
rs4252134
PLG
0.925 0.160 6 160732495 intron variant T/C snv 0.21 2
rs10783618
HOXC11 ; HOTAIR
1.000 0.160 12 53971491 intron variant T/C snv 0.51 1
rs2162440 1.000 0.160 18 37634043 intron variant A/G;T snv 1
rs2548861
WWOX
1.000 0.160 16 78624496 intron variant T/G snv 0.52 1
rs6430612 1.000 0.160 2 136248628 intergenic variant C/T snv 0.44 1
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs10818488
C5-OT1
0.776 0.360 9 120942809 regulatory region variant A/G snv 0.51 8
rs2900180
C5-OT1
0.827 0.280 9 120944104 regulatory region variant T/A;C snv 5