Disease: Inflammatory Bowel Diseases
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 8
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
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
rs11741861
ZNF300 ; IRGM
0.925 0.040 5 150898347 intron variant A/G snv 8.8E-02 3
rs1182188
GNA12
0.827 0.120 7 2830351 intron variant T/C snv 0.26 7
rs12718244
SPATA48
0.827 0.120 7 50136058 intron variant G/A snv 0.33 0.33 6
rs12942547
STAT3
0.807 0.200 17 42375526 intron variant A/G;T snv 6
rs13300218
NOTCH1
0.925 0.040 9 136505189 intron variant G/A snv 7.5E-02 3
rs13407913
ADCY3
0.827 0.120 2 24874775 intron variant A/G snv 0.54 6
rs1517352
STAT4
0.851 0.160 2 191066738 intron variant A/C snv 0.45 3
rs16940202 1.000 0.040 16 85980635 intron variant T/C snv 0.15 2
rs17119
LOC101928354
0.882 0.120 6 14719265 intron variant G/A snv 0.74 4
rs17229285
LOC105373831
1.000 0.040 2 198658398 intron variant C/A;T snv 2
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 8
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs17656349
CAMK2A
1.000 0.040 5 150226431 intron variant C/T snv 0.45 2
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 6
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 10