Disease: Multiple Sclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11074956 0.925 0.160 16 11243864 downstream gene variant G/T snv 0.34 2
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs12979659
VAV1
0.925 0.160 19 6825021 intron variant T/C snv 0.36 0.28 2
rs13315591
FAM107A ; LOC107984079
0.925 0.160 3 58571114 intron variant T/C snv 0.15 4
rs151719
HLA-DMB
0.925 0.160 6 32936123 non coding transcript exon variant C/T snv 0.72 2
rs17421624
TNXB
0.925 0.160 6 32098400 intron variant T/C snv 0.25 2
rs212389
LOC105378083 ; LOC112267968
0.925 0.160 6 159068759 non coding transcript exon variant G/A snv 0.60 4
rs2157051 0.925 0.160 6 32690847 regulatory region variant G/A snv 0.69 2
rs2524089
LOC112267902 ; HLA-B ; LINC02571
0.925 0.160 6 31298745 intron variant G/T snv 0.65 3
rs2524095
LINC02571 ; HLA-B ; LOC112267902
0.925 0.160 6 31298340 intron variant A/C snv 0.65 2
rs2546133
VAV1
0.925 0.160 19 6799666 intron variant T/A;C snv 2
rs2617822
VAV1
0.925 0.160 19 6801470 intron variant G/A;C snv 2
rs2621383 0.925 0.160 6 32791558 intergenic variant C/A snv 0.65 2
rs2621384 0.925 0.160 6 32791496 intergenic variant C/T snv 0.66 2
rs26232
MACIR
0.925 0.160 5 103261019 intron variant C/T snv 0.30 4
rs2849015 0.925 0.160 6 32231159 intergenic variant G/A snv 0.38 2
rs2857161 0.925 0.160 6 32791520 intergenic variant G/A snv 0.65 2
rs2894249
TSBP1-AS1 ; TSBP1
0.925 0.160 6 32358058 intron variant C/G;T snv 2
rs3129872
HLA-DRA
0.925 0.160 6 32439376 upstream gene variant A/T snv 0.24 2
rs3129877
HLA-DRA
0.925 0.160 6 32440820 intron variant G/A snv 0.26 2
rs3129932
TSBP1 ; TSBP1-AS1
0.925 0.160 6 32368350 intron variant G/C snv 0.76 3
rs3135342 0.925 0.160 6 32428838 intergenic variant G/T snv 0.24 2
rs3135377 0.925 0.160 6 32417622 regulatory region variant A/G snv 0.80 2
rs3135392
HLA-DRA
0.925 0.160 6 32441465 intron variant C/A snv 0.38 2