Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 8
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 6
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 6
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 5
rs3806156
BTNL2 ; TSBP1-AS1
0.827 0.280 6 32405921 intron variant G/A;T snv 5
rs7194
HLA-DRA
0.827 0.280 6 32444703 3 prime UTR variant G/A snv 0.61 5
rs9268645
HLA-DRA
0.827 0.360 6 32440750 intron variant C/G;T snv 5
rs615672
HLA-DRB1
0.851 0.240 6 32606394 intergenic variant G/A;C snv 5
rs9268858
HLA-DRB9
0.882 0.200 6 32461981 intron variant T/C snv 0.29 5
rs2076530
TSBP1-AS1 ; BTNL2
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 5
rs3129768 0.851 0.240 6 32627306 upstream gene variant G/T snv 0.76 4
rs6457620 0.882 0.200 6 32696222 intergenic variant G/C snv 0.52 4
rs9461799 0.807 0.360 6 32721752 downstream gene variant T/C snv 0.37 4
rs10947261
BTNL2 ; TSBP1-AS1
0.882 0.240 6 32405455 splice region variant G/T snv 0.11 4
rs9268856
HLA-DRB9
0.807 0.240 6 32461942 intron variant C/A;T snv 4
rs9268877
HLA-DRB9
0.827 0.200 6 32463370 intron variant A/G;T snv 4
rs539703
TSBP1-AS1 ; TSBP1
0.882 0.200 6 32320685 intron variant A/C;T snv 4
rs926591
TSBP1-AS1 ; TSBP1
0.882 0.200 6 32337913 intron variant C/A snv 0.33 4
rs4959093
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32345320 intron variant T/C snv 0.33 4
rs574710
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32320413 intron variant T/C snv 0.34 4
rs9268402
TSBP1 ; TSBP1-AS1
0.827 0.200 6 32373576 intron variant G/A snv 0.45 4
rs9368716
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32338313 intron variant G/A snv 0.39 4
rs2621416 0.882 0.280 6 32774091 intergenic variant T/C snv 0.26 3
rs2647046 0.882 0.200 6 32700559 TF binding site variant A/C snv 0.64 3