Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs928413
IL33
0.807 0.120 9 6213387 upstream gene variant G/A;C snv 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
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 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
rs2056626
CD247
0.882 0.080 1 167451188 intron variant T/G snv 0.30 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
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
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
rs3024655
IL4R
0.925 0.080 16 27358181 intron variant A/G;T snv 2
rs6866614
IRF1-AS1
0.925 0.080 5 132451445 intron variant A/G snv 0.71 2