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
rs2523535 0.851 0.200 6 31368473 intron variant A/G snv 0.32 7
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
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
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 6
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 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
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 5
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
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
rs3129720 0.851 0.280 6 32695854 intergenic variant T/C snv 0.76 4
rs3129768 0.851 0.240 6 32627306 upstream gene variant G/T snv 0.76 4
rs3130299 0.851 0.240 6 32235760 regulatory region variant A/G snv 0.24 4
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 4
rs6457620 0.882 0.200 6 32696222 intergenic variant G/C snv 0.52 4