Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
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
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs3761549
FOXP3
0.724 0.480 X 49260888 intron variant G/A snv 9.6E-02 18
rs2242652
TERT
0.724 0.400 5 1279913 intron variant G/A snv 0.18 16
rs4646536
CYP27B1
0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 14
rs2221903
IL21-AS1 ; IL21
0.752 0.360 4 122617757 intron variant C/T snv 0.77 12
rs12508721
IL21-AS1
0.742 0.360 4 122623509 intron variant C/T snv 0.24 11
rs907715
IL21
0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs2293152
STAT3
0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05 10
rs7453920
HLA-DQB2
0.752 0.440 6 32762235 intron variant A/G;T snv 10
rs2280883
FOXP3
0.827 0.280 X 49252667 intron variant T/C snv 0.30 9
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 9
rs13419896
EPAS1
0.776 0.240 2 46329206 intron variant G/A snv 0.10 8
rs4823173
PNPLA3
0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 8
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 7
rs9277378
HLA-DPB1 ; HLA-DPA1
0.827 0.320 6 33082502 intron variant A/G snv 0.40 5
rs10465885
LOC102723321 ; GJA5
0.882 0.080 1 147760632 intron variant T/A;C snv 4
rs2072906
PNPLA3
0.851 0.160 22 43937292 intron variant A/G snv 0.25 0.20 4
rs6715787
EPAS1
0.851 0.200 2 46349033 intron variant C/G;T snv 4
rs179009
TLR7
0.925 0.160 X 12885361 intron variant A/G;T snv 2
rs303218
LIPA ; IFIT1
1.000 0.080 10 89392836 intron variant G/A snv 0.18 1
rs35875104
CYP21A2 ; EHMT2
1.000 0.080 6 31888517 intron variant T/C snv 3.0E-02 3.0E-02 1