Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12722502
IL2RA
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 4
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 4
rs143326447
MIR4435-2HG ; SOCAR
0.925 0.080 2 111511155 intron variant T/C snv 0.11 4
rs17144046 0.882 0.120 10 8564051 intergenic variant A/G snv 0.28 4
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 4
rs2070901
FCER1G
0.882 0.120 1 161215268 non coding transcript exon variant G/T snv 0.32 4
rs3122929
STAT6
0.882 0.080 12 57115319 intron variant C/T snv 0.33 4
rs3749833
IRF1-AS1
0.925 0.080 5 132463934 non coding transcript exon variant T/C snv 0.23 4
rs4574025
TNFRSF11A
0.882 0.160 18 62342581 intron variant C/T snv 0.55 4
rs61894547
EMSY
0.882 0.160 11 76537586 intron variant C/T snv 3.1E-02 4
rs6594499 0.882 0.120 5 111134439 downstream gene variant C/A snv 0.56 4
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 4
rs9391997
IRF4
0.851 0.160 6 409119 3 prime UTR variant A/G snv 0.38 4
rs10036789 1.000 0.080 5 72400091 regulatory region variant C/A;G snv 3
rs10995245
ZNF365 ; LOC105378327
0.882 0.160 10 62631615 intron variant G/A;C snv 3
rs1102705 0.925 0.080 1 172731728 intergenic variant G/A snv 0.93 3
rs117137535
ARRDC1
0.882 0.120 9 137605991 intron variant G/A snv 2.7E-02 3
rs13277355 0.882 0.120 8 127765473 intergenic variant A/G snv 0.71 3
rs1655558
ITPKA
0.925 0.080 15 41495387 intron variant T/G snv 0.66 3
rs1775554 0.882 0.080 10 9012377 intergenic variant A/C snv 0.35 3
rs1950897
RAD51B
0.925 0.160 14 68293424 intron variant C/G;T snv 3
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 3
rs28406364
LOC102724596
1.000 0.080 17 49377145 intron variant C/T snv 0.33 3
rs4739738 0.882 0.120 8 80379410 intron variant G/A snv 0.60 3