Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs869025672 0.925 0.320 8 38414872 missense variant A/C;G snv 8.0E-06 1
rs121909633 1.000 0.080 8 38424546 missense variant A/G snv 2.9E-04 4.1E-04 1
rs121909634 1.000 0.080 8 38419676 missense variant A/G snv 1
rs121909638 0.882 0.280 8 38421853 missense variant A/G snv 1
rs397515481 1.000 0.280 8 38428048 missense variant A/G snv 1
rs869025669 1.000 0.280 8 38427970 missense variant A/G snv 1
rs121909630 0.925 0.160 8 38428043 missense variant C/A snv 1
rs398122946 1.000 0.280 8 38414889 missense variant C/A snv 1
rs121909637 0.882 0.240 8 38418249 missense variant C/A;T snv 1.2E-05; 2.0E-05 1
rs121909644 0.925 0.160 8 38413795 missense variant C/A;T snv 1
rs140254426 1.000 0.160 8 38429832 missense variant C/A;T snv 8.0E-06 1
rs760884357 1.000 0.160 8 38457435 missense variant C/G snv 4.0E-06 1
rs869025671 1.000 0.280 8 38414876 missense variant C/G snv 1
rs121909645 0.925 0.240 8 38424696 missense variant C/G;T snv 1
rs869025670 1.000 0.280 8 38417954 missense variant C/G;T snv 1
rs886037634 0.925 0.160 8 38421836 missense variant C/T snv 1
rs121909635 0.827 0.240 8 38426158 missense variant C/T snv 1
rs781328162 0.925 0.160 8 38413714 missense variant C/T snv 2.0E-05 3.5E-05 1
rs397515446 0.925 0.160 8 38414599 missense variant C/T snv 1
rs121909640 0.925 0.160 8 38429898 missense variant C/T snv 1
rs749758370 1.000 0.160 8 38417411 missense variant C/T snv 8.0E-06 7.0E-06 1
rs55642501 1.000 0.160 8 38429736 missense variant C/T snv 4.2E-04 1.7E-04 1
rs121909629 0.882 0.200 8 38415905 missense variant C/T snv 1
rs768957161 1.000 0.160 8 38414231 missense variant C/T snv 2.8E-05 2.8E-05 1
rs1131691929 1.000 0.160 8 38424628 missense variant C/T snv 1