Disease: Inflammatory Bowel Diseases
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 6
rs10761659 0.925 0.040 10 62685804 intron variant A/G snv 0.43 3
rs10800309 0.925 0.120 1 161502368 upstream gene variant A/G;T snv 2
rs11010067 0.925 0.040 10 35006503 downstream gene variant C/G snv 0.37 3
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs113010081 0.925 0.160 3 46415921 downstream gene variant T/C snv 7.3E-02 3
rs11554257 1.000 0.040 9 114842790 upstream gene variant T/C snv 0.13 2
rs11672983 1.000 0.040 19 54871595 upstream gene variant G/A snv 0.35 2
rs11742570 0.925 0.040 5 40410482 upstream gene variant T/C;G snv 3
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 3
rs12946510 0.851 0.160 17 39756124 downstream gene variant C/T snv 0.37 4
rs1569328 0.827 0.120 14 75275048 upstream gene variant C/T snv 0.12 6
rs16940202 1.000 0.040 16 85980635 intron variant T/C snv 0.15 2
rs16967103 0.827 0.120 15 38606989 intergenic variant T/C snv 0.22 6
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 6
rs17694108 0.925 0.040 19 33240645 regulatory region variant G/A snv 0.22 3
rs2050392 0.827 0.120 10 30402574 downstream gene variant G/A snv 0.45 6
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs2143178 0.827 0.120 22 39264824 intron variant T/C snv 0.19 6
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs2413583 0.925 0.040 22 39263768 intron variant C/T snv 0.19 3
rs2538470 0.827 0.120 7 148523356 intergenic variant A/G snv 0.61 6
rs2651244 1.000 0.040 1 70529879 upstream gene variant G/A snv 0.30 2
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 5