Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs1415346246 3 180659577 splice acceptor variant AACT/- delins 4.0E-06 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
rs1560086701 3 180641995 frameshift variant AT/- delins 1
rs1560090006 3 180652246 frameshift variant AGTGGCT/- del 1
rs1560092160 3 180659715 frameshift variant CT/- delins 1
rs1560092440 3 180660684 stop gained A/T snv 1
rs201780665 3 180642072 stop gained G/A;T snv 7.6E-05; 8.1E-06 1
rs577069249 3 180650140 intron variant T/C snv 5.0E-04 1
rs753580394 3 180644119 splice donor variant C/T snv 6.8E-06 1
rs756235547 3 180659582 splice acceptor variant T/C snv 1.2E-04 8.4E-05 1
rs769223754 3 180641993 missense variant C/A;T snv 7.0E-05; 4.3E-06 1
rs778577109 3 180661932 stop gained G/A snv 5.2E-06 7.0E-06 1