Disease: Celiac Disease
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
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 4