Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35919134
EIF4EP2
1.000 0.080 17 49424571 non coding transcript exon variant -/C delins 1
rs61376250
COL17A1
1.000 0.080 10 104055483 intron variant -/C;CAC;CACAC ins 1
rs6659932
IL12RB2
0.827 0.240 1 67336688 intron variant A/C snv 0.81 5
rs9268644
HLA-DRA
0.827 0.360 6 32440267 intron variant A/C snv 0.68 5
rs1054609
ZPBP2
0.925 0.160 17 39877024 3 prime UTR variant A/C snv 0.40 2
rs17574040
MAPT
1.000 0.080 17 46025499 3 prime UTR variant A/C snv 0.14 2
rs2158257
MAPT ; KANSL1
1.000 0.080 17 46026977 3 prime UTR variant A/C snv 0.14 2
rs860413 0.925 0.080 5 35942940 upstream gene variant A/C snv 0.23 2
rs11064157
LTBR
1.000 0.080 12 6383483 intron variant A/C snv 0.79 1
rs111413387 1.000 0.080 17 46267043 non coding transcript exon variant A/C snv 0.14 1
rs11209050
IL12RB2
1.000 0.080 1 67326053 intron variant A/C snv 0.68 1
rs137603 1.000 0.080 22 39298220 downstream gene variant A/C snv 0.50 1
rs17033015 1.000 0.080 4 102625147 intergenic variant A/C snv 0.65 1
rs1747677
COL17A1
1.000 0.080 10 104055483 intron variant A/C snv 0.75 1
rs4633993
PLCB1
1.000 0.080 20 8789461 intron variant A/C snv 0.90 1
rs5026476
MANBA
1.000 0.080 4 102633753 intron variant A/C snv 0.55 1
rs6812747
MANBA
1.000 0.080 4 102634260 intron variant A/C snv 0.55 1
rs735405
MANBA
1.000 0.080 4 102632759 intron variant A/C snv 0.55 1
rs75666751
MAPT
1.000 0.080 17 46012782 intron variant A/C snv 0.18 1
rs7628370
LOC105377110
1.000 0.080 3 59384874 intron variant A/C snv 0.22 1
rs77266933
MAPT
1.000 0.080 17 45949124 intron variant A/C snv 0.14 1
rs9906612
FBXL20
1.000 0.080 17 39391378 intron variant A/C snv 0.22 1
rs9971100
COL17A1
1.000 0.080 10 104066661 intron variant A/C snv 0.19 1
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs12150447
KANSL1
1.000 0.080 17 46050759 intron variant A/C;G snv 2