Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691741 1.000 0.160 13 51937305 missense variant T/G snv 7.0E-06 1
rs1333619338 1.000 0.160 13 51937315 missense variant C/T snv 1
rs753330854 1.000 0.160 13 51937332 missense variant C/G;T snv 4.0E-06; 1.2E-04 1
rs193922109 1.000 0.160 13 51937342 stop gained G/A snv 7.6E-05 8.4E-05 1
rs1057516228 1.000 0.160 13 51937349 frameshift variant C/- delins 1
rs1057516227 1.000 0.160 13 51937354 frameshift variant TG/- del 1
rs749380700 1.000 0.160 13 51937367 missense variant G/C snv 4.0E-06 1
rs377144951 1.000 0.160 13 51937383 missense variant A/G snv 1.4E-05 1
rs1057517233 1.000 0.160 13 51937395 splice acceptor variant T/C snv 1
rs749472361 1.000 0.160 13 51937484 missense variant G/A;C snv 3.6E-05; 4.0E-06 1
rs753044473 1.000 0.160 13 51937487 missense variant C/T snv 2.4E-05 1.4E-05 1
rs199821556 1.000 0.160 13 51937493 missense variant C/T snv 2.0E-04 1.5E-04 1
rs1340942427 1.000 0.160 13 51937495 missense variant G/T snv 1
rs776300396 1.000 0.160 13 51937502 missense variant C/T snv 2.0E-05 7.0E-06 1
rs373748155 1.000 0.160 13 51937516 missense variant G/A;C snv 8.0E-06 1.4E-05 1
rs762866453 1.000 0.160 13 51937520 missense variant C/T snv 3.6E-05 9.1E-05 1
rs755202606 1.000 0.160 13 51937537 missense variant C/G;T snv 8.0E-06 1
rs778914828 1.000 0.160 13 51937543 missense variant T/C snv 4.0E-06 1
rs758355520 1.000 0.160 13 51937561 missense variant G/A;T snv 2.4E-05 1
rs121907990 0.925 0.240 13 51937570 missense variant T/A;C snv 4.0E-06; 2.2E-04 2
rs1555283900 1.000 0.160 13 51937570 frameshift variant T/- delins 1
rs1314712150 1.000 0.160 13 51937577 missense variant C/T snv 4.0E-06 1
rs1057516740 1.000 0.160 13 51937579 frameshift variant T/- del 1
rs1555283916 1.000 0.160 13 51937579 missense variant T/G snv 1
rs121907992 1.000 0.160 13 51937583 missense variant C/T snv 2.8E-05 5.6E-05 1