Disease: Celiac Disease
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 3
rs13132308
IL21-AS1
0.807 0.160 4 122629959 intron variant A/G snv 0.10 6
rs17466626
LOC105369736 ; LRRK2
0.724 0.240 12 40366829 non coding transcript exon variant A/G snv 1.7E-02 14
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs4625
DAG1
0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs72743477
SMAD3
0.724 0.240 15 67171953 intron variant A/G snv 0.17 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 8
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs17885785
IGF2 ; IGF2-AS ; INS-IGF2
0.724 0.240 11 2146620 non coding transcript exon variant C/T snv 0.14 14
rs2066363
ADGRL2
0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs36001488
ATG16L1
0.724 0.240 2 233276621 intron variant C/T snv 0.44 14
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 15
rs755374 0.724 0.240 5 159402286 intron variant C/T snv 0.28 14
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17 14
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 15
rs114846446
LINC01250
0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14