Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs147897616
HLA-DQA1 ; LOC107986589
1.000 0.040 6 32638205 intron variant -/A;G ins 1
rs28986206
HLA-DRB1
1.000 0.040 6 32587634 intron variant -/AT ins 1
rs9282114
HLA-DQB1
1.000 0.040 6 32661903 non coding transcript exon variant -/C ins 1
rs565188555
TSBP1-AS1
1.000 0.040 6 32378631 intron variant -/GTAGATAG delins 1
rs199889539
LOC107986589 ; HLA-DQA1
1.000 0.040 6 32637642 intron variant -/T ins 1
rs372346302
HLA-DRB9
1.000 0.040 6 32466946 intron variant -/TA ins 7.0E-06 1
rs729302 0.827 0.160 7 128928906 intergenic variant A/C snv 0.28 6
rs113585425
HLA-DRB9
1.000 0.040 6 32465348 intron variant A/C snv 7.8E-02 1
rs12207473 1.000 0.040 6 32476553 upstream gene variant A/C snv 0.38 1
rs12858139
FLT1
1.000 0.040 13 28483931 intron variant A/C snv 0.44 1
rs13217512 1.000 0.040 6 32617919 intergenic variant A/C snv 4.8E-02 1
rs17191234
HLA-DRB1
1.000 0.040 6 32596904 intergenic variant A/C snv 0.34 1
rs17209887 1.000 0.040 6 32478274 upstream gene variant A/C snv 0.37 1
rs223498
MANBA
1.000 0.040 4 102730805 intron variant A/C snv 0.59 1
rs28366267
HLA-DRB1
1.000 0.040 6 32592004 upstream gene variant A/C snv 0.25 1
rs28366334
HLA-DRB1
1.000 0.040 6 32594118 upstream gene variant A/C snv 0.26 1
rs28383418
HLA-DQA2 ; HLA-DQA1 ; LOC107986589
1.000 0.040 6 32640760 intron variant A/C snv 0.11 1
rs3104415 1.000 0.040 6 32614800 intergenic variant A/C snv 0.31 1
rs481245
HLA-DRB1
1.000 0.040 6 32608337 intergenic variant A/C snv 0.41 1
rs9268409
TSBP1-AS1
1.000 0.040 6 32374862 intron variant A/C snv 0.24 1
rs9271492 1.000 0.040 6 32621345 regulatory region variant A/C snv 0.41 1
rs9581465
ATP8A2
1.000 0.040 13 25848944 intron variant A/C snv 0.14 1
rs9298814
IFNA17
0.790 0.160 9 21227623 missense variant A/C;G snv 0.12; 8.8E-06 7
rs6931332
HLA-B ; LOC112267902
1.000 0.040 6 31306468 intron variant A/C;G snv 1
rs79251508 1.000 0.040 6 32485855 intergenic variant A/C;G snv 1