Disease: Inflammatory Bowel Diseases
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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 10
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
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
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
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
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
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 7
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
rs17780256
LOC105371887 ; SLC39A11
0.827 0.120 17 72646784 3 prime UTR variant A/C snv 0.18 6
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
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
rs2050392 0.827 0.120 10 30402574 downstream gene variant G/A snv 0.45 6
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 17