Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10414065 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 4
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs10699671
NDFIP1
0.925 0.080 5 142139375 intron variant -/AGG delins 0.68 2
rs10795672 0.925 0.080 10 8735677 intergenic variant G/A;T snv 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
rs11650680 0.827 0.120 17 40422984 intergenic variant C/T snv 0.17 5
rs11715524
TFRC
0.925 0.080 3 196035621 intron variant G/A snv 0.54 3
rs11742240 0.925 0.080 5 35881274 downstream gene variant G/A;T snv 2
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs12470864
IL1RL1
0.925 0.080 2 102309902 upstream gene variant G/A snv 0.30 4
rs12617922 1.000 2 145399111 intergenic variant G/A snv 0.46 1
rs12722502
IL2RA
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 4
rs12788104 1.000 11 1129831 regulatory region variant A/G snv 0.55 1
rs1321859
LOC105377891
0.925 0.080 6 90301954 intron variant C/T snv 0.24 2
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 6
rs174621
FADS2
1.000 11 61862632 non coding transcript exon variant G/A;C snv 2
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs17668708
PTPRC
0.925 0.080 1 198671359 intron variant C/T snv 8.0E-02 2
rs1775554 0.882 0.080 10 9012377 intergenic variant A/C snv 0.35 3