Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13088318
FAM172BP
3 101523907 downstream gene variant A/G;T snv 0.24 1
rs1465325
IL1R1
2 102118091 intron variant A/G snv 0.15 1
rs1465324
IL1R1
2 102119152 intron variant G/A snv 0.18 1
rs12328681
IL1R1
2 102120407 intron variant G/T snv 0.18 1
rs10172039
IL1R1
2 102122325 intron variant C/A snv 0.18 1
rs12619383
IL1R1
2 102125258 intron variant A/G snv 0.15 1
rs12620132
IL1R1
2 102125655 intron variant A/G snv 0.15 1
rs13387400
IL1R1
2 102133560 intron variant G/A snv 0.15 1
rs2110727
IL1R1
2 102147834 intron variant G/A snv 0.18 1
rs1558641
IL1R1
0.925 0.080 2 102149405 intron variant G/A snv 0.13 3
rs1558640
IL1R1
2 102149418 intron variant G/A snv 0.16 1
rs949963
IL1R1
0.925 0.160 2 102153326 intron variant C/T snv 0.22 3
rs871657
IL1R1
1.000 0.080 2 102154881 intron variant C/T snv 0.22 2
rs2287048
IL1R1
2 102157539 intron variant C/T snv 0.13 1
rs3917285
IL1R1
2 102164706 intron variant T/A snv 6.9E-02 1
rs12474258
IL1RL2
2 102200235 intron variant C/T snv 0.63 1
rs1922302
IL1RL2
2 102202589 intron variant T/G snv 0.63 1
rs1922291
IL1RL2
2 102212357 intron variant A/G snv 0.63 1
rs6743219
IL1RL2
2 102215251 intron variant T/C snv 0.64 1
rs917994
IL1RL2
2 102220954 intron variant G/A snv 0.63 1
rs2302621
IL1RL2
2 102225664 intron variant G/T snv 0.63 1
rs1997502
IL1RL2
2 102227789 intron variant A/G;T snv 2
rs10167431
IL1RL2
2 102236342 intron variant T/C snv 0.55 1
rs10178214
IL1RL2
2 102242461 downstream gene variant G/T snv 0.24 1
rs13027294 2 102243614 downstream gene variant G/C;T snv 1