Disease: Multiple Sclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs11594656 0.776 0.240 10 6080046 intergenic variant T/A snv 0.18 9
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs11860650
ITGAM
0.882 0.120 16 31315385 intron variant C/T snv 0.14 3
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs2205960
TNFSF4
0.763 0.400 1 173222336 intergenic variant G/A;T snv 9
rs2294020
CCDC22
0.763 0.280 X 49246763 missense variant A/G;T snv 10
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs3027898
IRAK1
0.752 0.360 X 154010439 downstream gene variant C/A snv 11
rs3093023
LOC105378122 ; CCR6
0.851 0.160 6 167120802 intron variant G/A snv 0.34 7
rs3129871
HLA-DRA
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs3129882
HLA-DRA
0.807 0.240 6 32441753 intron variant G/A snv 0.56 6
rs35929052 0.827 0.160 16 85960878 downstream gene variant C/G;T snv 5
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs4963128
PHRF1
0.882 0.120 11 589564 intron variant T/C snv 0.64 3
rs5844572
MIF ; MIF-AS1
0.752 0.360 22 23893562 intron variant -/ATTC delins 11
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 11
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26