Disease: Multiple Sclerosis
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 2
rs151719
HLA-DMB
0.925 0.160 6 32936123 non coding transcript exon variant C/T snv 0.72 2
rs17421624
TNXB
0.925 0.160 6 32098400 intron variant T/C snv 0.25 2
rs2072633
CFB ; CYP21A2 ; NELFE
0.807 0.320 6 31951801 3 prime UTR variant A/G snv 0.59 2
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 2
rs2157051 0.925 0.160 6 32690847 regulatory region variant G/A snv 0.69 2
rs2524095
LINC02571 ; HLA-B ; LOC112267902
0.925 0.160 6 31298340 intron variant A/C snv 0.65 2
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
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
rs2894249
TSBP1-AS1 ; TSBP1
0.925 0.160 6 32358058 intron variant C/G;T snv 2
rs3129872
HLA-DRA
0.925 0.160 6 32439376 upstream gene variant A/T snv 0.24 2
rs3129877
HLA-DRA
0.925 0.160 6 32440820 intron variant G/A snv 0.26 2
rs3135342 0.925 0.160 6 32428838 intergenic variant G/T snv 0.24 2
rs3135377 0.925 0.160 6 32417622 regulatory region variant A/G snv 0.80 2
rs3135392
HLA-DRA
0.925 0.160 6 32441465 intron variant C/A snv 0.38 2
rs404890 0.925 0.160 6 32231090 intergenic variant C/A snv 0.35 2
rs486416
CYP21A2 ; EHMT2
0.925 0.160 6 31888293 intron variant G/A snv 0.77 0.76 2
rs5029937
TNFAIP3
0.882 0.160 6 137874014 intron variant G/T snv 0.13 2
rs6074022 0.851 0.240 20 46111557 TF binding site variant C/G;T snv 2
rs644045
CYP21A2 ; C2
0.851 0.240 6 31916180 intron variant A/G snv 0.72 2
rs6936204 0.925 0.160 6 32249315 intergenic variant T/C snv 0.70 2
rs9267873 0.925 0.160 6 32231575 intergenic variant C/G;T snv 2
rs9268429
TSBP1-AS1
0.925 0.160 6 32377275 intron variant A/G snv 0.24 2