Disease: Multiple Sclerosis
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 3
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs12928822
LOC105371082 ; RMI2
0.882 0.200 16 11310036 intron variant C/T snv 0.13 5
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs4263839
TNFSF15
0.807 0.160 9 114804160 intron variant A/G snv 0.75 3
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 5
rs1551398
LOC105375746
0.882 0.160 8 125527809 intron variant G/A snv 0.48 3
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 5
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs2188962
IRF1-AS1
0.882 0.160 5 132435113 intron variant C/T snv 0.29 4
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs11747270
IRGM
0.790 0.240 5 150879305 intron variant A/G snv 0.21 3
rs1736135
LOC101927745
0.851 0.160 21 15432901 intron variant T/C snv 0.33 4
rs1738074
LOC105378083 ; LOC107986664 ; TAGAP
0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 5
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 3
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 6
rs2274910
ITLN1
0.827 0.200 1 160882256 non coding transcript exon variant T/C snv 0.65 0.58 3
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 4
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 5