Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs12603332
LOC112268187 ; ORMDL3 ; LRRC3C
0.807 0.200 17 39926554 5 prime UTR variant T/C snv 0.49 7
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 7
rs928413
IL33
0.807 0.120 9 6213387 upstream gene variant G/A;C snv 7
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 6
rs4065275
ORMDL3
0.807 0.160 17 39924612 intron variant A/G;T snv 0.56 6
rs4795405
LRRC3C
0.851 0.160 17 39932164 intron variant T/A;C snv 6
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 6
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv 6
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 5
rs11650680 0.827 0.120 17 40422984 intergenic variant C/T snv 0.17 5
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs12365699 0.882 0.120 11 118872577 regulatory region variant G/A snv 0.12 5
rs16917204
BDNF-AS
0.827 0.160 11 27646808 intron variant G/C snv 0.17 5
rs2428494
HLA-B
0.827 0.160 6 31354420 intron variant T/A;C snv 5
rs2853209
ADAM33
0.827 0.200 20 3670825 intron variant T/A snv 0.41 5
rs3785356
IL4R
0.925 0.080 16 27337847 intron variant C/T snv 0.25 5
rs4512342
NRG1
0.827 0.120 8 32750356 intron variant T/G snv 0.12 5
rs55646091 0.925 0.080 11 76588387 upstream gene variant G/A snv 3.0E-02 5
rs5744455
CD14 ; TMCO6
0.882 0.160 5 140633722 upstream gene variant G/A;T snv 5
rs6871536
RAD50 ; TH2LCRR
0.827 0.160 5 132634182 intron variant T/C snv 0.24 5
rs6927172 0.851 0.120 6 137681038 intron variant C/A;G;T snv 5
rs705699
SUOX ; RAB5B
0.882 0.160 12 55991020 non coding transcript exon variant G/A snv 0.40 5
rs7936312 0.882 0.080 11 76582682 intergenic variant G/T snv 0.44 5