Disease: Celiac Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11217040 0.925 0.200 11 118809939 regulatory region variant C/A snv 0.19 2
rs17264332 0.925 0.200 6 137684378 intron variant A/G;T snv 2
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs424232 0.882 0.240 6 32240547 intergenic variant C/A;T snv 3
rs4821124 0.851 0.240 22 21625000 downstream gene variant T/C snv 0.19 4
rs62323881 0.925 0.200 4 122117140 regulatory region variant C/A;T snv 2
rs6696533 0.925 0.200 1 198764438 intergenic variant T/C snv 0.28 2
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs9275141 0.827 0.240 6 32683340 intergenic variant T/G snv 0.50 6
rs9357152 0.827 0.240 6 32697183 regulatory region variant A/G snv 0.24 5
rs11123810
AFF3
0.925 0.200 2 100142823 intron variant T/C snv 0.37 2
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 16
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs2043211
CARD8
0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs67676925
CCR3
0.925 0.200 3 46232768 intron variant T/C snv 5.5E-02 2
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs864537
CD247
0.925 0.200 1 167442147 intron variant A/G snv 0.29 4
rs2501432
CNR2
0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 16
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs879761216
CNR2
0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115