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
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
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
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
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
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 8
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 8
rs11229555
GLYAT
0.827 0.120 11 58641214 intron variant G/T snv 0.21 7
rs11230563
LOC105369326 ; CD6
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 6
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
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
rs11614178
IFNG-AS1 ; LOC107984526
0.827 0.120 12 68114342 intron variant G/A;T snv 0.26 6
rs11641184
LITAF
0.925 0.040 16 11610795 intron variant C/A snv 0.36 3