Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 4
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
rs3122929
STAT6
0.882 0.080 12 57115319 intron variant C/T snv 0.33 4
rs1775554 0.882 0.080 10 9012377 intergenic variant A/C snv 0.35 3
rs4739738 0.882 0.120 8 80379410 intron variant G/A snv 0.60 3
rs35441874
CLEC16A
0.882 0.120 16 11119164 intron variant T/A snv 0.19 3
rs11715524
TFRC
0.925 0.080 3 196035621 intron variant G/A snv 0.54 3
rs10795672 0.925 0.080 10 8735677 intergenic variant G/A;T snv 2
rs11742240 0.925 0.080 5 35881274 downstream gene variant G/A;T snv 2
rs190438685 0.925 0.080 4 39388825 intergenic variant C/T snv 6.2E-03 2
rs2381712 0.925 0.080 2 145387450 intergenic variant T/G snv 0.52 2
rs28415845 0.925 0.080 11 1151933 regulatory region variant T/C snv 0.58 2
rs35204956 0.925 0.080 8 80389778 intron variant A/-;AA;AAA delins 2
rs4771332 0.925 0.080 13 99418203 upstream gene variant T/A;C;G snv 2
rs540485182 0.925 0.080 5 110825774 intergenic variant -/A;AA;AAA delins 2
rs60227565 0.925 0.080 2 102275879 intergenic variant G/A;T snv 0.10 2
rs62557312 0.925 0.080 9 6047765 intron variant C/T snv 0.15 2
rs7099257 0.925 0.080 10 8468994 upstream gene variant T/A snv 0.49 2
rs58521088
BACH2
0.925 0.080 6 90275479 intron variant A/T snv 0.27 2
rs2056625
CD247
0.925 0.080 1 167451062 intron variant G/A snv 0.27 2
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
rs174621
FADS2
1.000 11 61862632 non coding transcript exon variant G/A;C snv 2