Disease: Inflammatory Bowel Diseases
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1182188
GNA12
0.827 0.120 7 2830351 intron variant T/C snv 0.26 7
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
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs12718244
SPATA48
0.827 0.120 7 50136058 intron variant G/A snv 0.33 0.33 6
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
rs12946510 0.851 0.160 17 39756124 downstream gene variant C/T snv 0.37 4
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
rs1569328 0.827 0.120 14 75275048 upstream gene variant C/T snv 0.12 6
rs16940202 1.000 0.040 16 85980635 intron variant T/C snv 0.15 2
rs16967103 0.827 0.120 15 38606989 intergenic variant T/C snv 0.22 6
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 6
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
rs17694108 0.925 0.040 19 33240645 regulatory region variant G/A snv 0.22 3
rs17780256
LOC105371887 ; SLC39A11
0.827 0.120 17 72646784 3 prime UTR variant A/C snv 0.18 6