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
rs1077773
KCCAT333
1.000 0.040 7 17403055 intron variant G/A;C snv 2
rs10800309 0.925 0.120 1 161502368 upstream gene variant A/G;T snv 2
rs11150589
ITGAL
1.000 0.040 16 30471173 upstream gene variant T/A;C;G snv 2
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 8
rs11230563
LOC105369326 ; CD6
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 6
rs113653754
HLA-DQB1-AS1
0.925 0.040 6 32658495 upstream gene variant C/A snv 3
rs11742570 0.925 0.040 5 40410482 upstream gene variant T/C;G snv 3
rs12103
INTS11 ; PUSL1 ; MIR6727
0.925 0.040 1 1312114 synonymous variant T/A;C;G snv 0.56 3
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 7
rs12942547
STAT3
0.807 0.200 17 42375526 intron variant A/G;T snv 6
rs17229285
LOC105373831
1.000 0.040 2 198658398 intron variant C/A;T snv 2
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs1811711
CCL20
1.000 0.040 2 227805760 5 prime UTR variant C/A;G snv 2
rs259964
ZNF831
0.827 0.120 20 59249254 intron variant A/G;T snv 6
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs35675666
PARK7
1.000 0.040 1 7961913 5 prime UTR variant G/C;T snv 2
rs4077515
CARD9
0.763 0.360 9 136372044 missense variant C/A;T snv 4.0E-06; 0.41 4
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs4380874 1.000 0.040 7 107839870 intergenic variant T/A;C;G snv 2
rs4409764 0.925 0.040 10 99524480 upstream gene variant T/A;G snv 3
rs4656958
ITLN1
0.925 0.040 1 160887174 upstream gene variant A/G;T snv 3
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs4946717
PRDM1
0.827 0.120 6 106026874 intron variant C/A;G;T snv 6