Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893755 0.851 0.200 3 87259959 missense variant G/A snv 5
rs754137696 0.925 0.160 3 57198797 missense variant A/C snv 1.9E-04 1.4E-05 2
rs777223697 0.925 0.160 3 57198802 stop gained A/T snv 8.0E-06 2
rs777833871 0.925 0.160 3 57198870 frameshift variant T/- del 1.4E-05 2
rs104893766 0.925 0.160 3 87262138 missense variant G/C snv 2
rs772390221 0.925 0.160 3 87261296 frameshift variant CTTTC/- delins 2
rs780359925 0.925 0.160 3 87259977 missense variant G/A snv 8.0E-06 2
rs606231411 1.000 0.120 3 87310484 intergenic variant C/T snv 1
rs104893754 1.000 0.120 3 87262161 stop gained G/A snv 4.0E-06 1
rs104893756 1.000 0.120 3 87262203 missense variant C/G;T snv 2.4E-05; 8.0E-06 1
rs104893757 1.000 0.120 3 87276392 missense variant G/A snv 1
rs104893758 1.000 0.120 3 87262098 missense variant A/G snv 4.0E-06 1
rs104893759 1.000 0.120 3 87264299 missense variant C/A;T snv 4.0E-06; 4.0E-06 1
rs104893760 1.000 0.120 3 87260022 stop gained C/A snv 1.6E-05 1
rs104893761 1.000 0.120 3 87264323 missense variant A/C snv 1
rs104893762 1.000 0.120 3 87260055 missense variant G/A snv 1
rs104893763 1.000 0.120 3 87264294 stop gained T/A snv 1
rs104893764 1.000 0.120 3 87260082 stop gained C/T snv 2.4E-05 7.0E-06 1
rs104893765 1.000 0.120 3 87262160 missense variant C/T snv 4.0E-06 1
rs1207179169 1.000 0.120 3 87262154 missense variant T/C snv 1
rs515726221 1.000 0.120 3 87261272 splice donor variant C/A snv 1
rs587776798 1.000 0.120 3 87260023 frameshift variant T/- delins 1
rs587776799 1.000 0.120 3 87259994 frameshift variant -/T delins 1
rs754584667 1.000 0.120 3 87264515 splice region variant G/A;C;T snv 1.6E-05 1