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
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 8
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 7
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs2736172
PRRC2A ; SNORA38
0.882 0.160 6 31623121 non coding transcript exon variant C/T snv 0.41 0.29 6
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 6
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 6
rs2076530
TSBP1-AS1 ; BTNL2
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 5
rs2395182
HLA-DRA
0.851 0.280 6 32445540 downstream gene variant G/T snv 0.76 5
rs3129871
HLA-DRA
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs3129882
HLA-DRA
0.807 0.240 6 32441753 intron variant G/A snv 0.56 5
rs3806156
BTNL2 ; TSBP1-AS1
0.827 0.280 6 32405921 intron variant G/A;T snv 5
rs3817963
TSBP1-AS1 ; BTNL2
0.776 0.360 6 32400310 intron variant T/C snv 0.25 5
rs615672
HLA-DRB1
0.851 0.240 6 32606394 intergenic variant G/A;C snv 5
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs6903608
HLA-DRB9
0.742 0.400 6 32460508 intron variant C/G;T snv 5