Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 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
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs2516400 0.827 0.320 6 31513328 upstream gene variant G/A snv 0.32 6
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs2857595 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 6
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 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
rs2219893 0.925 0.120 6 32801886 intergenic variant T/C snv 0.33 5
rs2395174 0.827 0.320 6 32437101 upstream gene variant T/G snv 0.24 5
rs2621373 0.925 0.120 6 32797353 TF binding site variant T/A;C;G snv 5
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 5
rs2858331 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 5
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 5
rs3130350 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 5
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs719654 0.925 0.120 6 32784362 intergenic variant G/A snv 0.21 5
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 5