Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
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
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
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv 6
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs9273349
HLA-DQB1-AS1
0.827 0.200 6 32658092 upstream gene variant T/C;G snv 6
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
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
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
rs10414065 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 4
rs12470864
IL1RL1
0.925 0.080 2 102309902 upstream gene variant G/A snv 0.30 4
rs12722502
IL2RA
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 4