Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs4648881 0.807 0.120 1 24870664 intergenic variant G/A snv 0.47 6
rs72698115
IL6R ; IL6R-AS1
0.807 0.120 1 154406893 intron variant A/C snv 7.2E-02 6
rs114940806
KLF17
0.882 0.120 1 44093000 intron variant A/G snv 5.4E-02 3
rs1823549 0.882 0.120 1 102682275 intergenic variant T/C snv 0.89 3
rs72632736 0.882 0.120 1 4389144 intergenic variant A/G snv 4.3E-02 3
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs10194635
LINC01104
0.807 0.120 2 100217755 intron variant T/A;G snv 6
rs45539732
STAT1
0.807 0.120 2 191009521 intron variant T/C snv 1.9E-02 6
rs11714843
TIMMDC1
0.807 0.120 3 119502217 intron variant T/A snv 0.15 6
rs79893749
CCR3
0.807 0.120 3 46212159 intron variant C/T snv 0.10 6
rs864089
PRICKLE2
0.882 0.120 3 64258442 intron variant T/C snv 0.22 3
rs1479924 0.807 0.120 4 122466445 intergenic variant G/A snv 0.76 6
rs6894249
IRF1-AS1
0.776 0.160 5 132461855 non coding transcript exon variant A/G snv 0.45 9
rs10213692
ANKRD55
0.807 0.120 5 56146422 intron variant T/C snv 0.17 6
rs27293
LNPEP
0.807 0.120 5 97021474 intron variant A/G;T snv 6
rs12517545
LINC01331
0.882 0.120 5 74384489 intron variant G/A snv 0.13 3
rs7775055 0.790 0.200 6 32690139 TF binding site variant T/C snv 6.2E-02 6
rs41291794 0.882 0.120 6 32457985 downstream gene variant A/T snv 7.5E-02 3
rs6946509 0.807 0.120 7 22769871 downstream gene variant T/A;C snv 6
rs73300638
JAZF1
0.807 0.120 7 28147725 intron variant A/C;G snv 6
rs1178121
HDAC9
0.882 0.120 7 18723029 intron variant C/A snv 0.31 3
rs1279094 0.882 0.120 9 11706771 intron variant T/C snv 0.43 3
rs2476491
IL2RA
0.776 0.240 10 6053447 intron variant A/T snv 0.25 6
rs7069750
FAS
0.807 0.120 10 89002619 non coding transcript exon variant G/C;T snv 0.50 6