Disease: Celiac Disease
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8