Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs928413
IL33
0.807 0.120 9 6213387 upstream gene variant G/A;C snv 7
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv 6
rs9273349
HLA-DQB1-AS1
0.827 0.200 6 32658092 upstream gene variant T/C;G snv 6
rs2428494
HLA-B
0.827 0.160 6 31354420 intron variant T/A;C snv 5
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 4
rs10795672 0.925 0.080 10 8735677 intergenic variant G/A;T snv 2
rs11255504
GATA3
0.925 0.080 10 8062378 intron variant A/G;T snv 2
rs11742240 0.925 0.080 5 35881274 downstream gene variant G/A;T snv 2
rs174621
FADS2
1.000 11 61862632 non coding transcript exon variant G/A;C snv 2
rs3024655
IL4R
0.925 0.080 16 27358181 intron variant A/G;T snv 2
rs35032408
CLEC16A
0.925 0.080 16 11121567 intron variant T/C;G snv 2
rs35204956 0.925 0.080 8 80389778 intron variant A/-;AA;AAA delins 2
rs4771332 0.925 0.080 13 99418203 upstream gene variant T/A;C;G snv 2
rs540485182 0.925 0.080 5 110825774 intergenic variant -/A;AA;AAA delins 2
rs56389811
HDAC7
1.000 12 47811575 intron variant C/A;T snv 1
rs190438685 0.925 0.080 4 39388825 intergenic variant C/T snv 6.2E-03 2
rs12722502
IL2RA
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 4
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs62322662 0.925 0.080 4 122438414 intergenic variant A/G snv 5.1E-02 4
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
rs17668708
PTPRC
0.925 0.080 1 198671359 intron variant C/T snv 8.0E-02 2
rs11088309
RUNX1
0.925 0.080 21 35092334 intron variant C/A;G snv 9.3E-02 2
rs60227565 0.925 0.080 2 102275879 intergenic variant G/A;T snv 0.10 2