Disease: Inflammatory Bowel Diseases
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4976646
RGS14
0.851 0.200 5 177361569 intron variant T/C snv 0.41 6
rs1250550
ZMIZ1
0.851 0.240 10 79300560 intron variant C/A snv 0.27 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
rs2688608 1.000 0.080 10 73898591 regulatory region variant G/T snv 0.44 2
rs630923
CXCR5
1.000 0.080 11 118883644 upstream gene variant C/A snv 0.13 2
rs6880778 1.000 0.080 5 40398994 intergenic variant A/G snv 0.58 2