Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs2858331 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 5
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 5
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 4
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 4
rs5000634 0.851 0.200 6 32695787 intergenic variant A/G snv 0.39 4
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 3
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 3
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 3
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3
rs13192471 0.925 0.160 6 32703326 downstream gene variant T/C snv 0.19 3
rs1456893 0.851 0.160 7 50230076 intron variant G/A snv 0.69 3
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 3
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 3
rs2006996 0.882 0.080 9 114830358 regulatory region variant T/C snv 7.2E-02 3