Source: GWASCAT ×
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 3
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv 6
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
rs1898671
TSLP
0.851 0.160 5 111072304 intron variant C/T snv 0.25 2
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs56062135
SMAD3
0.790 0.200 15 67163292 intron variant C/T snv 0.18 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 1
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 6
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 11
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 4
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 1