Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs1799969 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs1805094 0.716 0.440 1 65610269 missense variant G/C;T snv 0.16; 4.0E-06 16
rs10036748 0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs4917014 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 8
rs6590330 0.851 0.280 11 128441164 intergenic variant G/A;T snv 5
rs3788013 0.851 0.240 21 42421219 intron variant C/A snv 0.44 5
rs2298804 0.851 0.240 1 159304102 missense variant A/G;T snv 6.6E-03 4
rs13385731 0.882 0.200 2 33476823 intron variant T/C snv 6.3E-02 3
rs10847697 0.882 0.200 12 128814840 synonymous variant G/A snv 0.13 9.1E-02 3
rs4639966 0.925 0.120 11 118702810 intron variant T/C snv 0.23 2
rs16972959 0.925 0.120 16 23890055 intron variant G/A snv 0.15 2
rs16925200 1.000 0.040 9 7045058 intron variant T/C snv 4.3E-02 1
rs1195782955
MPO
1.000 0.040 17 58279411 synonymous variant C/T snv 7.0E-06 1