Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs56389811
HDAC7
1.000 12 47811575 intron variant C/A;T snv 1
rs2544026
HDAC7
0.925 0.080 12 47792780 non coding transcript exon variant T/A snv 0.19 2
rs11650680 0.827 0.120 17 40422984 intergenic variant C/T snv 0.17 5
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs28635831
COG6
0.925 0.080 13 39745817 intron variant A/G snv 0.27 2
rs190438685 0.925 0.080 4 39388825 intergenic variant C/T snv 6.2E-03 2
rs11742240 0.925 0.080 5 35881274 downstream gene variant G/A;T snv 2
rs11088309
RUNX1
0.925 0.080 21 35092334 intron variant C/A;G snv 9.3E-02 2
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs10414065 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 4
rs4491851
GLB1
0.925 0.080 3 33042493 intron variant G/A snv 0.50 2
rs28407950
HLA-DQB1-AS1
0.925 0.080 6 32658571 upstream gene variant C/T snv 0.29 2
rs9273349
HLA-DQB1-AS1
0.827 0.200 6 32658092 upstream gene variant T/C;G snv 6
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 8
rs2428494
HLA-B
0.827 0.160 6 31354420 intron variant T/A;C snv 5
rs1117490
TRIM26
0.925 0.080 6 30202733 intron variant T/C snv 0.24 2
rs3024655
IL4R
0.925 0.080 16 27358181 intron variant A/G;T snv 2
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs17668708
PTPRC
0.925 0.080 1 198671359 intron variant C/T snv 8.0E-02 2
rs11715524
TFRC
0.925 0.080 3 196035621 intron variant G/A snv 0.54 3
rs2056626
CD247
0.882 0.080 1 167451188 intron variant T/G snv 0.30 5
rs2056625
CD247
0.925 0.080 1 167451062 intron variant G/A snv 0.27 2
rs12617922 1.000 2 145399111 intergenic variant G/A snv 0.46 1