Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs2234767
FAS ; ACTA2
0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs3761549
FOXP3
0.724 0.480 X 49260888 intron variant G/A snv 9.6E-02 18
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs1179251
IL22 ; LOC105369818
0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 14
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs17375018
C1orf141 ; IL23R
0.790 0.360 1 67189464 intron variant G/A snv 0.29 7
rs3792876
SLC22A4
0.790 0.280 5 132301616 intron variant C/T snv 6.9E-02 7
rs1534422
MIR3681HG
0.827 0.160 2 12500615 intron variant G/A snv 0.52 6
rs17445836 0.851 0.320 16 85984057 intron variant G/A snv 0.15 5
rs179247
TSHR
0.882 0.160 14 80966202 intron variant A/G snv 0.40 5
rs2160322
MAGI2
0.851 0.160 7 78462650 intron variant G/A;C snv 5
rs6479778
ARID5B
0.827 0.200 10 61929318 intron variant T/C;G snv 5
rs706779
IL2RA
0.827 0.160 10 6056861 intron variant T/C snv 0.48 5