Disease: Crohn Disease
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 7
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs660895
HLA-DRB1
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 6
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs2858331 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 5
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 5
rs7765379 0.827 0.280 6 32713151 upstream gene variant T/G snv 0.10 3
rs9275328 0.851 0.240 6 32699045 intergenic variant C/T snv 0.16 3
rs2071538
TAP1 ; PSMB9
0.925 0.160 6 32850901 intron variant G/A snv 0.18 0.17 2