Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs545854 0.882 0.160 8 10002570 intron variant G/C snv 0.85 2
rs2453626
RGS22
1.000 0.080 8 100125669 intron variant T/A;C snv 1
rs949963
IL1R1
0.925 0.160 2 102153326 intron variant C/T snv 0.22 2
rs871657
IL1R1
1.000 0.080 2 102154881 intron variant C/T snv 0.22 2
rs10189629 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 2
rs11692065 1.000 0.080 2 102267515 intergenic variant C/T snv 0.15 2
rs11674302 1.000 0.080 2 102270668 intergenic variant T/C snv 0.16 2
rs12479210
IL1RL1 ; IL18R1
1.000 0.080 2 102332701 intron variant C/A;T snv 1
rs3771180
IL18R1 ; IL1RL1
1.000 0.080 2 102337157 5 prime UTR variant G/A;T snv 2
rs13431828
IL1RL1 ; IL18R1
0.925 0.160 2 102338193 5 prime UTR variant C/T snv 0.18 2
rs13408569
IL1RL1 ; IL18R1
1.000 0.080 2 102338596 intron variant G/C snv 0.18 2
rs13408661
IL1RL1 ; IL18R1
1.000 0.080 2 102338622 intron variant G/A snv 0.18 2
rs10173081
IL1RL1 ; IL18R1
1.000 0.080 2 102340888 intron variant C/T snv 0.18 2
rs1420101
IL1RL1 ; IL18R1
0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 2
rs3771175
IL1RL1 ; IL18R1
0.925 0.080 2 102343750 3 prime UTR variant T/A snv 0.18 2
rs10208293
IL1RL1 ; IL18R1
0.882 0.160 2 102349850 intron variant G/A snv 0.33 1
rs10197862
IL18R1 ; IL1RL1
0.925 0.120 2 102350089 intron variant A/G snv 0.18 2
rs10204137
IL18R1 ; IL1RL1
0.925 0.160 2 102351752 missense variant A/G;T snv 0.34 1
rs10192157
IL18R1 ; IL1RL1
1.000 0.080 2 102351896 missense variant C/T snv 0.34 0.46 2
rs10206753
IL18R1 ; IL1RL1
1.000 0.080 2 102351902 missense variant T/C;G snv 0.34; 4.0E-06 2
rs9807989
IL18R1
1.000 0.080 2 102354740 intron variant T/C;G snv 0.46 1
rs3755276
IL18R1
0.925 0.120 2 102361999 intron variant C/T snv 0.45 2
rs1362348
IL18R1
1.000 0.080 2 102368164 intron variant C/G snv 0.45 2
rs3771166
IL18R1
1.000 0.080 2 102369762 intron variant G/A;T snv 2
rs3755266
IL18RAP
1.000 0.080 2 102426252 intron variant G/A snv 0.55 1