Disease: Crohn Disease
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 7
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17 7
rs4976646
RGS14
0.851 0.200 5 177361569 intron variant T/C snv 0.41 6
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 6
rs1250550
ZMIZ1
0.851 0.240 10 79300560 intron variant C/A snv 0.27 5
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 5
rs12946510 0.851 0.160 17 39756124 downstream gene variant C/T snv 0.37 4
rs17119
LOC101928354
0.882 0.120 6 14719265 intron variant G/A snv 0.74 4
rs6074022 0.851 0.240 20 46111557 TF binding site variant C/G;T snv 3
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 3
rs12722489
IL2RA
0.882 0.160 10 6060049 intron variant C/T snv 0.11 2
rs4613763 0.851 0.240 5 40392626 regulatory region variant T/C snv 0.14 2
rs9292777 0.925 0.120 5 40437846 regulatory region variant C/T snv 0.60 2
rs9891119
STAT3
0.882 0.120 17 42355962 intron variant A/C snv 0.36 2
rs9989735
SP140
0.925 0.120 2 230250739 intron variant G/C;T snv 2