Disease: Multiple Sclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs11074956 0.925 0.160 16 11243864 downstream gene variant G/T snv 0.34 2
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 6
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs2157051 0.925 0.160 6 32690847 regulatory region variant G/A snv 0.69 2
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs2395173 0.882 0.240 6 32437082 upstream gene variant A/G snv 0.62 3
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs2621383 0.925 0.160 6 32791558 intergenic variant C/A snv 0.65 2
rs2621384 0.925 0.160 6 32791496 intergenic variant C/T snv 0.66 2
rs2647046 0.882 0.200 6 32700559 TF binding site variant A/C snv 0.64 3
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs2849015 0.925 0.160 6 32231159 intergenic variant G/A snv 0.38 2
rs2857161 0.925 0.160 6 32791520 intergenic variant G/A snv 0.65 2
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs3115576 0.882 0.200 6 32249073 intergenic variant T/A snv 0.41 3
rs3129720 0.851 0.280 6 32695854 intergenic variant T/C snv 0.76 4
rs3129768 0.851 0.240 6 32627306 upstream gene variant G/T snv 0.76 4
rs3130299 0.851 0.240 6 32235760 regulatory region variant A/G snv 0.24 4
rs3130311 0.882 0.200 6 32249590 intergenic variant A/G;T snv 3
rs3134926 0.882 0.200 6 32232370 intergenic variant C/A;G snv 3
rs3135338 0.882 0.240 6 32433440 regulatory region variant C/T snv 0.62 3
rs3135342 0.925 0.160 6 32428838 intergenic variant G/T snv 0.24 2