Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs56062135
SMAD3
0.790 0.200 15 67163292 intron variant C/T snv 0.18 8
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 8
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv 6
rs1898671
TSLP
0.851 0.160 5 111072304 intron variant C/T snv 0.25 5
rs2056626
CD247
0.882 0.080 1 167451188 intron variant T/G snv 0.30 5
rs2428494
HLA-B
0.827 0.160 6 31354420 intron variant T/A;C snv 5
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs12722502
IL2RA
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 4
rs3122929
STAT6
0.882 0.080 12 57115319 intron variant C/T snv 0.33 4
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs11715524
TFRC
0.925 0.080 3 196035621 intron variant G/A snv 0.54 3
rs35441874
CLEC16A
0.882 0.120 16 11119164 intron variant T/A snv 0.19 3
rs4739738 0.882 0.120 8 80379410 intron variant G/A snv 0.60 3
rs10699671
NDFIP1
0.925 0.080 5 142139375 intron variant -/AGG delins 0.68 2
rs11088309
RUNX1
0.925 0.080 21 35092334 intron variant C/A;G snv 9.3E-02 2
rs1117490
TRIM26
0.925 0.080 6 30202733 intron variant T/C snv 0.24 2
rs11178648
TSPAN8
0.925 0.080 12 71139430 intron variant C/T snv 0.29 2
rs11255504
GATA3
0.925 0.080 10 8062378 intron variant A/G;T snv 2
rs1321859
LOC105377891
0.925 0.080 6 90301954 intron variant C/T snv 0.24 2
rs17668708
PTPRC
0.925 0.080 1 198671359 intron variant C/T snv 8.0E-02 2
rs2056625
CD247
0.925 0.080 1 167451062 intron variant G/A snv 0.27 2
rs28635831
COG6
0.925 0.080 13 39745817 intron variant A/G snv 0.27 2