Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12788104 1.000 11 1129831 regulatory region variant A/G snv 0.55 1
rs58521088
BACH2
0.925 0.080 6 90275479 intron variant A/T snv 0.27 2
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
rs35441874
CLEC16A
0.882 0.120 16 11119164 intron variant T/A snv 0.19 3
rs35032408
CLEC16A
0.925 0.080 16 11121567 intron variant T/C;G snv 2
rs28635831
COG6
0.925 0.080 13 39745817 intron variant A/G snv 0.27 2
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs174621
FADS2
1.000 11 61862632 non coding transcript exon variant G/A;C snv 2
rs11255504
GATA3
0.925 0.080 10 8062378 intron variant A/G;T snv 2
rs4491851
GLB1
0.925 0.080 3 33042493 intron variant G/A snv 0.50 2
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs2544026
HDAC7
0.925 0.080 12 47792780 non coding transcript exon variant T/A snv 0.19 2
rs56389811
HDAC7
1.000 12 47811575 intron variant C/A;T snv 1
rs2428494
HLA-B
0.827 0.160 6 31354420 intron variant T/A;C snv 5
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 8
rs9273349
HLA-DQB1-AS1
0.827 0.200 6 32658092 upstream gene variant T/C;G snv 6
rs28407950
HLA-DQB1-AS1
0.925 0.080 6 32658571 upstream gene variant C/T snv 0.29 2
rs12470864
IL1RL1
0.925 0.080 2 102309902 upstream gene variant G/A snv 0.30 4
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs12722502
IL2RA
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 4
rs928413
IL33
0.807 0.120 9 6213387 upstream gene variant G/A;C snv 7
rs3024655
IL4R
0.925 0.080 16 27358181 intron variant A/G;T snv 2
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8