Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs770861172 0.827 0.160 2 195857582 missense variant C/T snv 4.0E-06 7.0E-06 6
rs142371860 0.925 0.160 2 26421396 stop gained C/A;T snv 3.9E-04 3
rs146412095 2 26450086 splice donor variant G/A;T snv 8.1E-05; 4.1E-06 1
rs745800344 2 26444221 splice acceptor variant G/T snv 8.0E-06 7.0E-06 1
rs138815960 0.925 0.160 3 50345533 splice donor variant A/C snv 2.7E-04 2.1E-04 3
rs200913791 0.925 0.160 3 50342473 missense variant A/G snv 2.0E-04 3.5E-05 3
rs397515392 1.000 0.120 3 180661860 splice donor variant C/G snv 1.6E-04 7.0E-05 2
rs587778820 1.000 0.120 3 180619334 frameshift variant T/- delins 2.6E-05 1.4E-05 2
rs587778822 1.000 0.120 3 180651496 frameshift variant T/- delins 1.4E-05 2
rs773801386 1.000 0.120 3 180654861 frameshift variant GT/- delins 4.2E-05 2
rs1007345781 3 180616604 frameshift variant GT/- delins 8.7E-06 2.8E-05 1
rs1210953680 3 180652161 splice donor variant A/T snv 1
rs1275367324 3 180651409 frameshift variant C/- del 5.9E-06 1
rs1285431486 3 180642111 frameshift variant C/- del 4.0E-06 1
rs1297857806 3 50342917 splice donor variant C/T snv 4.0E-06 1
rs1415346246 3 180659577 splice acceptor variant AACT/- delins 4.0E-06 1
rs1553800956 3 180616551 stop gained C/A snv 1
rs1553803540 3 180641992 splice donor variant C/T snv 1
rs1553804100 3 180647254 intron variant T/C snv 1
rs1553804209 3 180648215 frameshift variant -/T delins 1
rs1553804220 3 180648285 frameshift variant C/- del 1
rs1553804640 3 180651533 splice acceptor variant C/- delins 1
rs1553805740 3 180659694 frameshift variant -/GT delins 1
rs1553805885 3 180660635 frameshift variant C/- del 1
rs1560079213 3 180616697 splice acceptor variant T/- del 1