Disease: Hodgkin Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
rs3129882
HLA-DRA
0.807 0.240 6 32441753 intron variant G/A snv 0.56 6
rs9296015 0.851 0.280 6 32251212 upstream gene variant G/A snv 0.22 4
rs6901221 0.925 0.160 6 33130499 downstream gene variant A/C snv 0.13 2