Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1898671
TSLP
0.851 0.160 5 111072304 intron variant C/T snv 0.25 5
rs10414065 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 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
rs11178648
TSPAN8
0.925 0.080 12 71139430 intron variant C/T snv 0.29 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
rs190438685 0.925 0.080 4 39388825 intergenic variant C/T snv 6.2E-03 2
rs28407950
HLA-DQB1-AS1
0.925 0.080 6 32658571 upstream gene variant C/T snv 0.29 2
rs62557312 0.925 0.080 9 6047765 intron variant C/T snv 0.15 2
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 8
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs705699
SUOX ; RAB5B
0.882 0.160 12 55991020 non coding transcript exon variant G/A snv 0.40 5
rs12470864
IL1RL1
0.925 0.080 2 102309902 upstream gene variant G/A snv 0.30 4
rs11715524
TFRC
0.925 0.080 3 196035621 intron variant G/A snv 0.54 3
rs4739738 0.882 0.120 8 80379410 intron variant G/A snv 0.60 3
rs2056625
CD247
0.925 0.080 1 167451062 intron variant G/A snv 0.27 2
rs4491851
GLB1
0.925 0.080 3 33042493 intron variant G/A snv 0.50 2
rs12617922 1.000 2 145399111 intergenic variant G/A snv 0.46 1
rs928413
IL33
0.807 0.120 9 6213387 upstream gene variant G/A;C snv 7
rs174621
FADS2
1.000 11 61862632 non coding transcript exon variant G/A;C snv 2
rs10795672 0.925 0.080 10 8735677 intergenic variant G/A;T snv 2
rs11742240 0.925 0.080 5 35881274 downstream gene variant G/A;T snv 2
rs60227565 0.925 0.080 2 102275879 intergenic variant G/A;T snv 0.10 2