Disease: Inflammatory Bowel Diseases
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1049526
BRD2
0.925 0.040 6 32981027 3 prime UTR variant C/T snv 0.93 3
rs10761659 0.925 0.040 10 62685804 intron variant A/G snv 0.43 3
rs1077773
KCCAT333
1.000 0.040 7 17403055 intron variant G/A;C snv 2
rs10781499
CARD9
0.925 0.040 9 136371953 synonymous variant G/A snv 0.41 0.38 3
rs10797432
LOC100996583
1.000 0.040 1 2569899 downstream gene variant C/T snv 0.51 2
rs11010067 0.925 0.040 10 35006503 downstream gene variant C/G snv 0.37 3
rs11064881
CIT
1.000 0.040 12 119709120 intron variant G/A snv 5.0E-02 3
rs111456533
EEF1AKMT2
1.000 0.040 10 124750812 intron variant G/A snv 0.18 2
rs11150589
ITGAL
1.000 0.040 16 30471173 upstream gene variant T/A;C;G snv 2
rs113653754
HLA-DQB1-AS1
0.925 0.040 6 32658495 upstream gene variant C/A snv 3
rs11548656
PLCG2
1.000 0.040 16 81883307 missense variant A/G snv 2.5E-02 2.7E-02 2
rs11554257 1.000 0.040 9 114842790 upstream gene variant T/C snv 0.13 2
rs11581607
IL23R
0.925 0.040 1 67242007 intron variant G/A snv 4.6E-02 4
rs11641184
LITAF
0.925 0.040 16 11610795 intron variant C/A snv 0.36 3
rs11672983 1.000 0.040 19 54871595 upstream gene variant G/A snv 0.35 2
rs11741861
ZNF300 ; IRGM
0.925 0.040 5 150898347 intron variant A/G snv 8.8E-02 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
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 3
rs13300218
NOTCH1
0.925 0.040 9 136505189 intron variant G/A snv 7.5E-02 3
rs16940202 1.000 0.040 16 85980635 intron variant T/C snv 0.15 2
rs17229285
LOC105373831
1.000 0.040 2 198658398 intron variant C/A;T snv 2
rs17656349
CAMK2A
1.000 0.040 5 150226431 intron variant C/T snv 0.45 2
rs17694108 0.925 0.040 19 33240645 regulatory region variant G/A snv 0.22 3
rs1811711
CCL20
1.000 0.040 2 227805760 5 prime UTR variant C/A;G snv 2