Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs60227565 0.925 0.080 2 102275879 intergenic variant G/A;T snv 0.10 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
rs540485182 0.925 0.080 5 110825774 intergenic variant -/A;AA;AAA delins 2
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs1898671
TSLP
0.851 0.160 5 111072304 intron variant C/T snv 0.25 5
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
rs1784775
SIK2
0.925 0.080 11 111601736 upstream gene variant T/C snv 0.59 2
rs12788104 1.000 11 1129831 regulatory region variant A/G snv 0.55 1
rs28415845 0.925 0.080 11 1151933 regulatory region variant T/C snv 0.58 2
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 6
rs62322662 0.925 0.080 4 122438414 intergenic variant A/G snv 5.1E-02 4
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs6866614
IRF1-AS1
0.925 0.080 5 132451445 intron variant A/G snv 0.71 2
rs10699671
NDFIP1
0.925 0.080 5 142139375 intron variant -/AGG delins 0.68 2
rs2381712 0.925 0.080 2 145387450 intergenic variant T/G snv 0.52 2
rs12617922 1.000 2 145399111 intergenic variant G/A snv 0.46 1
rs2056625
CD247
0.925 0.080 1 167451062 intron variant G/A snv 0.27 2
rs2056626
CD247
0.882 0.080 1 167451188 intron variant T/G snv 0.30 5
rs11715524
TFRC
0.925 0.080 3 196035621 intron variant G/A snv 0.54 3
rs17668708
PTPRC
0.925 0.080 1 198671359 intron variant C/T snv 8.0E-02 2
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs3024655
IL4R
0.925 0.080 16 27358181 intron variant A/G;T snv 2