Disease: Inflammatory Bowel Diseases
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 9
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
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 8
rs11938228
TLR2
0.882 0.120 4 153700794 intron variant C/A;T snv 4
rs1250546
ZMIZ1
0.925 0.080 10 79272775 intron variant A/G snv 0.36 3
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 7
rs13407913
ADCY3
0.827 0.120 2 24874775 intron variant A/G snv 0.54 6
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 7
rs2024092
SBNO2
0.827 0.120 19 1124032 intron variant G/A snv 0.24 0.26 6
rs2143178 0.827 0.120 22 39264824 intron variant T/C snv 0.19 6
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18 7
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 9
rs259964
ZNF831
0.827 0.120 20 59249254 intron variant A/G;T snv 6
rs26528
IL27
0.807 0.200 16 28506388 intron variant T/C snv 0.43 9
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84 6
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 9
rs34779708
CREM
0.827 0.120 10 35177257 intron variant T/G snv 0.33 6
rs3766606
PARK7
0.827 0.120 1 7962137 intron variant G/T snv 0.22 6
rs3776414
DAP
0.827 0.120 5 10689450 intron variant T/G snv 0.48 6