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
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 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
rs1179251
IL22 ; LOC105369818
0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs3118470
IL2RA
0.752 0.360 10 6059750 intron variant T/A;C snv 10
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs2903692
CLEC16A
0.807 0.360 16 11144926 intron variant G/A snv 0.33 6
rs17445836 0.851 0.320 16 85984057 intron variant G/A snv 0.15 5
rs3788013
UBASH3A
0.851 0.240 21 42421219 intron variant C/A snv 0.44 5
rs6479778
ARID5B
0.827 0.200 10 61929318 intron variant T/C;G snv 5
rs4840568
BLK
0.882 0.160 8 11493510 intron variant G/A snv 0.32 4
rs12492609
TMEM39A
0.882 0.040 3 119435715 intron variant C/T snv 0.14 3
rs17593222
STAT3
0.925 0.120 17 42360972 intron variant C/G snv 6.1E-02 3
rs2071400
TPO
0.882 0.120 2 1412867 intron variant C/T snv 0.11 3
rs2276886
CXCL9
0.882 0.120 4 76007275 intron variant C/A;T snv 3
rs2280381 0.882 0.080 16 85985027 intron variant C/T snv 0.64 3
rs661561
TNFAIP3
0.882 0.200 6 137876194 intron variant A/C snv 0.62 0.50 3
rs7629750
TMEM39A
0.882 0.040 3 119455829 intron variant A/G snv 0.45 3
rs2048722
TPO
0.925 2 1492028 intron variant A/G snv 0.51 2
rs2618431
FAM167A
0.925 0.120 8 11466955 intron variant A/G snv 0.87 2