Disease: Ulcerative Colitis
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 7
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 4
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 3
rs7554511
INAVA
0.925 0.040 1 200908434 intron variant C/A snv 0.22 3
rs907611
LSP1
0.882 0.160 11 1852842 upstream gene variant G/A snv 0.26 3
rs10781499
CARD9
0.925 0.040 9 136371953 synonymous variant G/A snv 0.41 0.38 2
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 2
rs35675666
PARK7
1.000 0.040 1 7961913 5 prime UTR variant G/C;T snv 2
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 2
rs6871626 0.851 0.160 5 159399784 intron variant C/A;G snv 0.29 2
rs7134599
IFNG-AS1 ; LOC107984526
1.000 0.040 12 68106295 intron variant G/A snv 0.32 2
rs7608910
PUS10
0.827 0.120 2 60977721 intron variant A/G snv 0.37 2
rs941823
LINC00598
0.827 0.120 13 40439840 intron variant T/C snv 0.77 2