Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7759742 1.000 0.040 6 32413959 regulatory region variant T/A;G snv 0.56 3
rs12069782
C1orf141
1.000 0.040 1 67134418 intron variant C/T snv 0.82 2
rs1891467
TGFB2
0.925 0.040 1 218406643 intron variant A/G snv 0.34 2
rs206530
LOC105371989
0.925 0.040 18 10394467 downstream gene variant T/C snv 0.70 2
rs2213585
HLA-DRA
1.000 0.040 6 32445373 downstream gene variant G/A snv 0.61 2
rs2213586
HLA-DRA
1.000 0.040 6 32445317 downstream gene variant A/G snv 0.61 2
rs2523587 1.000 0.040 6 31359623 upstream gene variant T/C snv 0.71 2
rs2524139
LINC02571 ; HLA-B ; LOC112267902
1.000 0.040 6 31296356 intron variant G/C;T snv 2
rs2524142
HLA-B ; LINC02571
1.000 0.040 6 31295745 intron variant C/A;G snv 2
rs2524143
LINC02571 ; HLA-B
1.000 0.040 6 31295733 intron variant T/C snv 0.81 2
rs28366301
HLA-DRB1
1.000 0.040 6 32593106 upstream gene variant G/A snv 0.26 2
rs2894204
HLA-C
1.000 0.040 6 31269284 intron variant C/A;T snv 2
rs3093958
LINC01149
1.000 0.040 6 31442744 intron variant A/G snv 7.0E-02 2
rs3117116
TSBP1-AS1 ; BTNL2
1.000 0.040 6 32399240 intron variant G/A snv 0.87 2
rs3130968 1.000 0.040 6 31097294 regulatory region variant C/G;T snv 2
rs5007259 0.925 0.040 6 32411324 upstream gene variant T/C snv 0.55 2
rs7195
HLA-DRA
1.000 0.040 6 32444762 3 prime UTR variant A/G snv 0.61 2
rs7754768 1.000 0.040 6 32452402 regulatory region variant C/T snv 0.56 2
rs9266257
HLA-B
1.000 0.040 6 31358109 upstream gene variant G/A;C snv 2
rs9268658
HLA-DRA
1.000 0.040 6 32442939 intron variant G/A;C snv 2
rs9271585 1.000 0.040 6 32623102 regulatory region variant C/A snv 0.27 2
rs9271762 1.000 0.040 6 32626251 upstream gene variant T/G snv 2
rs10162249
ATP8A2
1.000 0.040 13 25849519 intron variant T/C snv 0.14 1
rs10467674
ATP8A2
1.000 0.040 13 25854100 intron variant T/A snv 0.14 1
rs1050045
OS9
1.000 0.040 12 57721488 3 prime UTR variant T/C snv 0.40 1