Disease: Multiple Sclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11175593
LRRK2 ; LRRK2-DT ; LINC02471 ; LOC105369735
0.882 0.160 12 40208138 non coding transcript exon variant C/T snv 2.8E-02 3
rs11190140
NKX2-3 ; LINC01475
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 6
rs1456893 0.851 0.160 7 50230076 intron variant G/A snv 0.69 4
rs1551398
LOC105375746
0.882 0.160 8 125527809 intron variant G/A snv 0.48 3
rs1736135
LOC101927745
0.851 0.160 21 15432901 intron variant T/C snv 0.33 4
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 3
rs2188962
IRF1-AS1
0.882 0.160 5 132435113 intron variant C/T snv 0.29 5
rs3828309
ATG16L1
0.882 0.160 2 233271764 intron variant A/G snv 0.42 3
rs4263839
TNFSF15
0.807 0.160 9 114804160 intron variant A/G snv 0.75 7
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 5
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs11584383
MROH3P
0.827 0.200 1 200966738 downstream gene variant T/C snv 0.24 5
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs12928822
LOC105371082 ; RMI2
0.882 0.200 16 11310036 intron variant C/T snv 0.13 5
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv 5
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 7
rs13314993
LOC105377022
0.882 0.200 3 32973977 regulatory region variant G/C;T snv 5
rs17035378
PLEK ; LOC101927723
0.882 0.200 2 68371823 intron variant T/A;C snv 5
rs2274910
ITLN1
0.827 0.200 1 160882256 non coding transcript exon variant T/C snv 0.65 0.58 6
rs2816316
LOC105371664
0.882 0.200 1 192567683 intron variant C/A snv 0.79 5
rs296547
MROH3P
0.882 0.200 1 200923009 intron variant T/C snv 0.53 5
rs3748816
MMEL1
0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 7