Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs863225228 0.925 0.280 8 93787884 missense variant C/T snv 2
rs863225231 0.925 0.280 8 93782455 missense variant C/G snv 7.0E-06 2
rs863225232 0.925 0.280 8 93782402 missense variant C/T snv 7.0E-06 2
rs863225233 0.925 0.280 8 93815365 missense variant T/G snv 2
rs863225234 0.925 0.280 8 93808922 missense variant A/C snv 2
rs116647652 1.000 0.160 8 93786285 stop gained C/A;T snv 8.0E-06 1
rs1554557920 1.000 0.160 8 93803677 splice donor variant TGAGTAATGTAA/G delins 1
rs267607114 1.000 0.160 8 93793256 missense variant G/A snv 4.0E-06 7.0E-06 1
rs267607118 1.000 0.160 8 93755044 stop gained C/T snv 4.0E-06 7.0E-06 1
rs751309268 1.000 0.160 8 93755854 stop gained C/A;T snv 8.1E-06 1
rs751517725 1.000 0.160 8 93803652 stop gained C/G;T snv 4.0E-06; 4.0E-06 1
rs762543032 1.000 0.160 8 93755798 missense variant C/T snv 4.3E-06 1
rs772437766 1.000 0.160 8 93755799 missense variant C/G;T snv 8.6E-06 1
rs775256658 1.000 0.160 8 93780985 splice region variant A/G snv 4.0E-06 1
rs781383498 1.000 0.160 8 93799649 missense variant A/C snv 8.0E-06 2.1E-05 1
rs863225224 1.000 0.160 8 93793299 splice region variant A/G snv 1
rs863225229 1.000 0.160 8 93780608 missense variant A/G snv 1
rs863225230 1.000 0.160 8 93804807 missense variant C/A snv 1
rs863225236 1.000 0.160 8 93815341 missense variant G/A snv 1
rs863225237 1.000 0.160 8 93782410 stop gained G/A;C;T snv 4.0E-06; 4.0E-06; 8.0E-06 1
rs863225238 1.000 0.160 8 93797456 missense variant C/T snv 4.0E-06; 4.0E-06 1
rs863225239 1.000 0.160 8 93809166 splice region variant G/A snv 4.0E-06 1
rs863225240 1.000 0.160 8 93803689 splice region variant G/- del 1