Disease: Multiple Sclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5844572
MIF ; MIF-AS1
0.752 0.360 22 23893562 intron variant -/ATTC delins 11
rs2524095
LINC02571 ; HLA-B ; LOC112267902
0.925 0.160 6 31298340 intron variant A/C snv 0.65 2
rs2647046 0.882 0.200 6 32700559 TF binding site variant A/C snv 0.64 3
rs3129871
HLA-DRA
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs437179
SKIV2L ; CYP21A2
0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78 3
rs6568431
ATG5
0.790 0.320 6 106140931 intron variant A/C snv 0.61 7
rs104895271
TNFRSF1A
0.851 0.240 12 6334161 missense variant A/C;G snv 1.6E-04; 4.8E-05 6
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs3134603
PPT2-EGFL8 ; PPT2
0.851 0.360 6 32158225 non coding transcript exon variant A/C;G;T snv 4
rs539703
TSBP1-AS1 ; TSBP1
0.882 0.200 6 32320685 intron variant A/C;T snv 4
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs9267954 0.882 0.200 6 32245275 regulatory region variant A/C;T snv 3
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 7
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs2040406
HLA-DQA1
0.882 0.240 6 32635230 intron variant A/G snv 0.23 3
rs2072633
CFB ; CYP21A2 ; NELFE
0.807 0.320 6 31951801 3 prime UTR variant A/G snv 0.59 6
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