Disease: Celiac Disease
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs212388
LOC112267968 ; LOC105378083
0.827 0.240 6 159069404 intron variant C/G;T snv 4
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4