Disease: Multiple Sclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104895271
TNFRSF1A
0.851 0.240 12 6334161 missense variant A/C;G snv 1.6E-04; 4.8E-05 6
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs17235409
SLC11A1
0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs17879469
HLA-DRB1
0.763 0.360 6 32584333 missense variant C/G snv 1.3E-05 9
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1862513
RETN
0.763 0.360 19 7668907 upstream gene variant C/G;T snv 11
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 14
rs2227956
HSPA1L
0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 12
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2232365
FOXP3
0.716 0.480 X 49259429 intron variant T/C snv 16
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2501432
CNR2
0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 16
rs2546133
VAV1
0.925 0.160 19 6799666 intron variant T/A;C snv 2
rs2617822
VAV1
0.925 0.160 19 6801470 intron variant G/A;C snv 2
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs2894249
TSBP1-AS1 ; TSBP1
0.925 0.160 6 32358058 intron variant C/G;T snv 2
rs3027898
IRAK1
0.752 0.360 X 154010439 downstream gene variant C/A snv 11
rs3129941
TSBP1 ; TSBP1-AS1
0.882 0.240 6 32369909 missense variant A/G;T snv 0.81 3
rs3130311 0.882 0.200 6 32249590 intergenic variant A/G;T snv 3
rs3134603
PPT2-EGFL8 ; PPT2
0.851 0.360 6 32158225 non coding transcript exon variant A/C;G;T snv 4
rs3134926 0.882 0.200 6 32232370 intergenic variant C/A;G snv 3
rs3134943
AGPAT1 ; MIR6833 ; RNF5
0.882 0.240 6 32179984 intron variant T/A;C snv 0.89 3