Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 7
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17 7
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 6
rs35667974
IFIH1
0.776 0.280 2 162268127 missense variant T/C snv 1.1E-02 1.2E-02 6
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 5
rs3774937
NFKB1
0.776 0.280 4 102513096 intron variant T/C snv 0.26 5
rs582757
TNFAIP3
0.776 0.320 6 137876687 intron variant C/T snv 0.70 5
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs11230563
LOC105369326 ; CD6
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 6
rs2236379
PRKCQ
0.790 0.160 10 6485181 missense variant G/A snv 0.31 0.30 6
rs2812378
CCL21
0.790 0.200 9 34710263 intron variant G/A;C snv 6
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 5
rs1860545
TNFRSF1A
0.790 0.200 12 6337611 intron variant G/A snv 0.31 5
rs35018800
TYK2
0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 5
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 10
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 8
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 7
rs11117431 0.807 0.160 16 85981710 intron variant A/G snv 0.18 6
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 6
rs1267499
LOC101928354
0.807 0.160 6 14715651 intron variant T/A;C snv 6
rs12942547
STAT3
0.807 0.200 17 42375526 intron variant A/G;T snv 6