Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121909627 0.776 0.200 8 38424690 missense variant G/C snv 4.0E-06 2
rs1085307879 1.000 0.160 8 38414183 missense variant T/C snv 1
rs1131691929 1.000 0.160 8 38424628 missense variant C/T snv 1
rs121909628 0.925 0.160 8 38414892 stop gained G/A;C snv 1
rs121909629 0.882 0.200 8 38415905 missense variant C/T snv 1
rs121909630 0.925 0.160 8 38428043 missense variant C/A snv 1
rs121909635 0.827 0.240 8 38426158 missense variant C/T snv 1
rs121909637 0.882 0.240 8 38418249 missense variant C/A;T snv 1.2E-05; 2.0E-05 1
rs121909638 0.882 0.280 8 38421853 missense variant A/G snv 1
rs121909640 0.925 0.160 8 38429898 missense variant C/T snv 1
rs121909641 0.763 0.520 8 38419720 missense variant G/A snv 1
rs121909642 0.925 0.160 8 38414174 missense variant G/A snv 1
rs121909644 0.925 0.160 8 38413795 missense variant C/A;T snv 1
rs121909645 0.925 0.240 8 38424696 missense variant C/G;T snv 1
rs140254426 1.000 0.160 8 38429832 missense variant C/A;T snv 8.0E-06 1
rs1554570706 0.925 0.200 8 38429808 missense variant G/A snv 1
rs397515444 0.925 0.160 8 38417975 missense variant G/A;T snv 4.0E-06 1
rs397515445 0.807 0.280 8 38414263 missense variant T/C snv 1
rs397515446 0.925 0.160 8 38414599 missense variant C/T snv 1
rs55642501 1.000 0.160 8 38429736 missense variant C/T snv 4.2E-04 1.7E-04 1
rs727505369 0.925 0.160 8 38424624 missense variant T/C snv 1
rs727505373 0.925 0.160 8 38429744 missense variant T/C snv 1
rs747842199 1.000 0.160 8 38429694 missense variant C/T snv 2.8E-05 1.4E-05 1
rs749758370 1.000 0.160 8 38417411 missense variant C/T snv 8.0E-06 7.0E-06 1
rs760884357 1.000 0.160 8 38457435 missense variant C/G snv 4.0E-06 1