Disease: Multiple Sclerosis
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 3
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 5
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 4
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 3
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 7
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 3
rs11747270
IRGM
0.790 0.240 5 150879305 intron variant A/G snv 0.21 3
rs1738074
LOC105378083 ; LOC107986664 ; TAGAP
0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 5
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 6
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs4819388
ICOSLG
0.790 0.240 21 44227538 3 prime UTR variant T/C snv 5
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 8
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 6
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs3764147
LACC1
0.807 0.280 13 43883789 missense variant A/G snv 0.28 0.27 4