Disease: Hodgkin Disease
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 8
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 8
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 7
rs2534657
MICB
0.882 0.200 6 31504682 intron variant C/T snv 0.15 6
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 5
rs6903608
HLA-DRB9
0.742 0.400 6 32460508 intron variant C/G;T snv 5
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 5
rs707928
VWA7
0.827 0.320 6 31774813 intron variant A/G snv 0.47 4
rs9296015 0.851 0.280 6 32251212 upstream gene variant G/A snv 0.22 4
rs2763979
HSPA1B
0.827 0.360 6 31826815 upstream gene variant C/T snv 0.45 3
rs805294
LY6G6C ; MPIG6B
0.882 0.240 6 31720440 intron variant A/G snv 0.48 3
rs4959089 0.925 0.200 6 32251948 upstream gene variant A/G snv 0.22 2