Disease: Inflammatory Bowel Diseases
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 5
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs727088
CD226
0.790 0.400 18 69863203 3 prime UTR variant G/A snv 0.47 2
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 8
rs12942547
STAT3
0.807 0.200 17 42375526 intron variant A/G;T snv 6
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 6
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18 6
rs26528
IL27
0.807 0.200 16 28506388 intron variant T/C snv 0.43 6
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 7
rs3749171
GPR35
0.807 0.120 2 240630275 missense variant C/T snv 0.16; 9.4E-06 0.19 6
rs56167332 0.807 0.160 5 159400761 intron variant C/A;T snv 6
rs7556897 0.807 0.120 2 227795396 intergenic variant C/G;T snv 6
rs11229555
GLYAT
0.827 0.120 11 58641214 intron variant G/T snv 0.21 7
rs11614178
IFNG-AS1 ; LOC107984526
0.827 0.120 12 68114342 intron variant G/A;T snv 0.26 6
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
rs13407913
ADCY3
0.827 0.120 2 24874775 intron variant A/G snv 0.54 6
rs1569328 0.827 0.120 14 75275048 upstream gene variant C/T snv 0.12 6
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
rs17780256
LOC105371887 ; SLC39A11
0.827 0.120 17 72646784 3 prime UTR variant A/C snv 0.18 6
rs2024092
SBNO2
0.827 0.120 19 1124032 intron variant G/A snv 0.24 0.26 6
rs2050392 0.827 0.120 10 30402574 downstream gene variant G/A snv 0.45 6
rs2143178 0.827 0.120 22 39264824 intron variant T/C snv 0.19 6
rs2538470 0.827 0.120 7 148523356 intergenic variant A/G snv 0.61 6