Disease: Celiac Disease
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs13132308
IL21-AS1
0.807 0.160 4 122629959 intron variant A/G snv 0.10 6
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs7042370
LURAP1L-AS1 ; LURAP1L
0.724 0.240 9 12785074 intron variant T/C snv 0.58 14
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 8
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11741255
IRF1-AS1
0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs755374 0.724 0.240 5 159402286 intron variant C/T snv 0.28 14
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs6689858
CRB1
0.724 0.240 1 197406337 intron variant T/C snv 0.39 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs17885785
IGF2 ; IGF2-AS ; INS-IGF2
0.724 0.240 11 2146620 non coding transcript exon variant C/T snv 0.14 14
rs36001488
ATG16L1
0.724 0.240 2 233276621 intron variant C/T snv 0.44 14