Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886037891 0.790 0.160 7 55155917 missense variant G/T snv 4.0E-06 7
rs587776671 0.790 0.160 10 87864506 frameshift variant AA/-;AAA delins 7
rs121909221 0.790 0.160 10 87952135 missense variant T/A snv 7
rs121909222 0.742 0.240 10 87933127 missense variant A/G snv 7
rs121909226 0.790 0.160 10 87925557 missense variant T/C snv 7
rs121909228 0.790 0.160 10 87957984 stop gained G/T snv 7
rs1554825165 0.790 0.160 10 87957872 stop gained C/A snv 7
rs1554825530 0.790 0.160 10 87960957 frameshift variant -/CT;TTCT ins 7
rs1554825643 0.790 0.160 10 87961107 frameshift variant C/- delins 7
rs1554897854 0.790 0.160 10 87931042 splice acceptor variant AGTT/- delins 7
rs1554897889 0.790 0.160 10 87931094 splice region variant G/A;T snv 7
rs1554898083 0.790 0.160 10 87933057 frameshift variant -/T delins 7
rs1554898085 0.790 0.160 10 87933061 frameshift variant -/AAACC delins 7
rs1554898242 0.790 0.160 10 87933252 splice donor variant G/T snv 7
rs1554898244 0.790 0.160 10 87933253 splice donor variant T/C;G snv 7
rs1554900675 0.790 0.160 10 87952263 splice region variant A/T snv 7
rs397515374 0.790 0.160 10 87952159 stop gained TA/AT mnv 7
rs587776666 0.790 0.160 10 87933106 frameshift variant ACAAT/- del 7
rs587776669 0.790 0.160 10 87957914 frameshift variant A/- del 7
rs587776670 0.790 0.160 10 87952211 frameshift variant C/- del 7.0E-06 7
rs587776672 0.790 0.160 10 87960893 splice acceptor variant G/- delins 7
rs587776673 0.790 0.160 10 87952130 frameshift variant C/- delins 7
rs1060500126 0.790 0.160 10 87933223 missense variant A/C;G snv 8
rs1114167621 0.790 0.160 10 87931045 splice acceptor variant G/A;C;T snv 8
rs1114167622 0.790 0.160 10 87952260 splice donor variant G/C snv 8