Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 4
rs1775554 0.882 0.080 10 9012377 intergenic variant A/C snv 0.35 3
rs35441874
CLEC16A
0.882 0.120 16 11119164 intron variant T/A snv 0.19 3
rs4739738 0.882 0.120 8 80379410 intron variant G/A snv 0.60 3
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs12470864
IL1RL1
0.925 0.080 2 102309902 upstream gene variant G/A snv 0.30 4
rs62322662 0.925 0.080 4 122438414 intergenic variant A/G snv 5.1E-02 4
rs11715524
TFRC
0.925 0.080 3 196035621 intron variant G/A snv 0.54 3
rs10699671
NDFIP1
0.925 0.080 5 142139375 intron variant -/AGG delins 0.68 2
rs10795672 0.925 0.080 10 8735677 intergenic variant G/A;T snv 2
rs11088309
RUNX1
0.925 0.080 21 35092334 intron variant C/A;G snv 9.3E-02 2
rs1117490
TRIM26
0.925 0.080 6 30202733 intron variant T/C snv 0.24 2
rs11178648
TSPAN8
0.925 0.080 12 71139430 intron variant C/T snv 0.29 2
rs11255504
GATA3
0.925 0.080 10 8062378 intron variant A/G;T snv 2
rs11742240 0.925 0.080 5 35881274 downstream gene variant G/A;T snv 2
rs1321859
LOC105377891
0.925 0.080 6 90301954 intron variant C/T snv 0.24 2
rs17668708
PTPRC
0.925 0.080 1 198671359 intron variant C/T snv 8.0E-02 2
rs1784775
SIK2
0.925 0.080 11 111601736 upstream gene variant T/C snv 0.59 2
rs190438685 0.925 0.080 4 39388825 intergenic variant C/T snv 6.2E-03 2
rs2056625
CD247
0.925 0.080 1 167451062 intron variant G/A snv 0.27 2
rs2381712 0.925 0.080 2 145387450 intergenic variant T/G snv 0.52 2
rs2544026
HDAC7
0.925 0.080 12 47792780 non coding transcript exon variant T/A snv 0.19 2
rs28407950
HLA-DQB1-AS1
0.925 0.080 6 32658571 upstream gene variant C/T snv 0.29 2
rs28415845 0.925 0.080 11 1151933 regulatory region variant T/C snv 0.58 2