Disease: Multiple Sclerosis
Source: ALL
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 0.93 121
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 8
rs3825932
CTSH
0.827 0.360 15 78943104 intron variant T/C snv 0.50 6
rs9268858
HLA-DRB9
0.882 0.200 6 32461981 intron variant T/C snv 0.29 5
rs10411936
EPS15L1
1.000 0.080 19 16437564 intron variant A/G snv 0.63 3
rs2524089
LOC112267902 ; HLA-B ; LINC02571
0.925 0.160 6 31298745 intron variant G/T snv 0.65 3
rs3129932
TSBP1 ; TSBP1-AS1
0.925 0.160 6 32368350 intron variant G/C snv 0.76 3