Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894701 0.925 0.040 19 920542 stop gained C/T snv 7.0E-06 1
rs104894702 0.925 0.040 19 920746 stop lost T/A;C snv 6.8E-05 1
rs121909640 0.925 0.160 8 38429898 missense variant C/T snv 1
rs121918340 0.925 0.040 9 137449656 missense variant T/C snv 1
rs781328162 0.925 0.160 8 38413714 missense variant C/T snv 2.0E-05 3.5E-05 1
rs606231407 1.000 0.040 10 101770613 missense variant C/T snv 1.6E-05 2
rs727505367 1.000 0.040 4 67753986 missense variant A/C snv 1.4E-05 2
rs727505370 1.000 0.040 8 38414840 missense variant A/G snv 2
rs727505371 1.000 0.040 8 38421840 frameshift variant AG/- delins 4.0E-06 2
rs727505374 1.000 0.040 X 8539744 stop gained G/A snv 2
rs104893838 1.000 0.040 4 67753950 missense variant G/A;C;T snv 4.0E-06; 4.0E-06; 1.6E-05 1
rs104893839 1.000 0.040 4 67744659 missense variant G/T snv 1
rs104893840 1.000 0.040 4 67753832 missense variant A/T snv 1
rs104893841 1.000 0.040 4 67740526 stop gained A/T snv 1
rs104893847 1.000 0.040 4 67740508 missense variant G/A snv 1
rs1391808526 1.000 0.040 4 67754089 missense variant G/C snv 4.0E-06 7.0E-06 1
rs144900788 1.000 0.040 4 67753900 missense variant G/A;T snv 1.3E-03 1
rs281865427 1.000 0.040 4 67754305 missense variant GA/TT mnv 1
rs28933074 1.000 0.040 4 67740616 missense variant T/C snv 4.0E-06 1.4E-05 1
rs515726219 1.000 0.040 4 67754242 splice donor variant T/C snv 3.6E-05 7.0E-06 1
rs727505375 1.000 0.040 4 103658329 stop gained C/T snv 4.0E-06 7.0E-06 1
rs727505377 1.000 0.040 8 38414001 missense variant A/G snv 1
rs774317793 1.000 0.040 4 67754283 missense variant T/C snv 1.9E-04 2.1E-05 1
rs797044452 1.000 0.040 4 67744788 splice acceptor variant C/T snv 1
rs886907903 1.000 0.040 4 67754226 missense variant A/C snv 1