Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3749171
GPR35
0.807 0.120 2 240630275 missense variant C/T snv 0.16; 9.4E-06 0.19 1
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 1
rs9468925
HLA-B
0.851 0.040 6 31291060 intron variant G/A snv 0.44 1
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 1
rs3213094
IL12B ; LOC107986469
0.925 0.080 5 159323761 intron variant C/G;T snv 0.26 1
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 1
rs13132308
IL21-AS1
0.807 0.160 4 122629959 intron variant A/G snv 0.10 1
rs10889676
IL23R
0.827 0.120 1 67256884 intron variant C/A;T snv 1
rs1343151
IL23R
0.752 0.400 1 67253446 intron variant G/A snv 0.41 1
rs26528
IL27
0.807 0.200 16 28506388 intron variant T/C snv 0.43 1
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 1
rs7849191
JAK2
0.882 0.120 9 4988761 intron variant C/T snv 0.50 1
rs849135
JAZF1
0.925 0.120 7 28156794 intron variant G/A snv 0.40 1
rs17716942
KCNH7
0.925 0.040 2 162404181 intron variant T/C snv 9.6E-02 1
rs9297145
KPNA7
0.827 0.120 7 99161494 intergenic variant C/A snv 0.67 1
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19 1
rs62149416
LINC01185
0.925 0.040 2 60856371 intron variant T/C snv 0.26 1
rs11121129
LINC01714
1.000 0.040 1 8208035 intron variant G/A snv 0.26 1
rs11230563
LOC105369326 ; CD6
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 1
rs367569
LOC105371082 ; RMI2
0.807 0.120 16 11271643 intron variant C/T snv 0.32 1
rs10979182
LOC105376214
1.000 0.040 9 108054739 regulatory region variant A/G snv 0.44 1
rs6809854
LOC105376976
1.000 0.040 3 18742931 intron variant A/G snv 0.19 1
rs1047781
LOC105447645 ; FUT2
0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 1