Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs6296
HTR1B ; LOC105377864
0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs2076530
TSBP1-AS1 ; BTNL2
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 17
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs3087456
CIITA ; LOC105371080
0.742 0.480 16 10877045 intron variant G/A snv 0.53 14
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 11
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 10
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 8
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 7
rs7194
HLA-DRA
0.827 0.280 6 32444703 3 prime UTR variant G/A snv 0.61 7
rs9461799 0.807 0.360 6 32721752 downstream gene variant T/C snv 0.37 6
rs615672
HLA-DRB1
0.851 0.240 6 32606394 intergenic variant G/A;C snv 6
rs9268856
HLA-DRB9
0.807 0.240 6 32461942 intron variant C/A;T snv 6
rs6457620 0.882 0.200 6 32696222 intergenic variant G/C snv 0.52 5
rs9469220 0.827 0.160 6 32690533 TF binding site variant G/A snv 0.53 5
rs3806156
BTNL2 ; TSBP1-AS1
0.827 0.280 6 32405921 intron variant G/A;T snv 5
rs9268645
HLA-DRA
0.827 0.360 6 32440750 intron variant C/G;T snv 5
rs9268858
HLA-DRB9
0.882 0.200 6 32461981 intron variant T/C snv 0.29 5
rs9268877
HLA-DRB9
0.827 0.200 6 32463370 intron variant A/G;T snv 5
rs9268402
TSBP1 ; TSBP1-AS1
0.827 0.200 6 32373576 intron variant G/A snv 0.45 5
rs2621416 0.882 0.280 6 32774091 intergenic variant T/C snv 0.26 4
rs3129768 0.851 0.240 6 32627306 upstream gene variant G/T snv 0.76 4
rs10947261
BTNL2 ; TSBP1-AS1
0.882 0.240 6 32405455 splice region variant G/T snv 0.11 4
rs2289702
CTSH
0.851 0.120 15 78944951 missense variant C/T snv 9.3E-02 7.8E-02 4