Disease: Multiple Sclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 7
rs12979659
VAV1
0.925 0.160 19 6825021 intron variant T/C snv 0.36 0.28 2
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs13315591
FAM107A ; LOC107984079
0.925 0.160 3 58571114 intron variant T/C snv 0.15 4
rs1678542
KIF5A
0.790 0.320 12 57574932 intron variant C/G snv 0.42 9
rs17388568
ADAD1
0.827 0.280 4 122408207 intron variant G/A snv 0.20 6
rs17421624
TNXB
0.925 0.160 6 32098400 intron variant T/C snv 0.25 2
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs2040406
HLA-DQA1
0.882 0.240 6 32635230 intron variant A/G snv 0.23 3
rs2076533
BTNL2 ; TSBP1-AS1
0.882 0.200 6 32395750 intron variant C/T snv 0.40 3
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 14
rs2232365
FOXP3
0.716 0.480 X 49259429 intron variant T/C snv 16
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
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
rs26232
MACIR
0.925 0.160 5 103261019 intron variant C/T snv 0.30 4