Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs1131691021 0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs121918453 0.732 0.280 12 112450394 missense variant G/A;C;T snv 19
rs2229080
DCC
0.742 0.320 18 52906232 missense variant C/A;G snv 0.45 16
rs2279343 0.776 0.200 19 41009358 missense variant A/G snv 0.13 8
rs3211371 0.827 0.080 19 41016810 missense variant C/A;T snv 1.2E-04; 8.8E-02 6
rs1057519696
ALK
1.000 0.040 2 29214054 missense variant C/T snv 5
rs80357989 0.882 0.200 17 43094680 frameshift variant -/TAATGAG delins 4
rs1196220479 0.851 0.120 11 102223635 missense variant G/A snv 4.0E-06 4
rs774829510 0.882 0.040 9 21971046 missense variant C/A;T snv 3
rs1057519793 0.882 0.040 5 177095551 missense variant T/A snv 3
rs766121173 0.882 0.040 5 177095625 missense variant G/A snv 1.1E-04 6.3E-05 3
rs1057519792 1.000 0.040 5 177095415 missense variant C/A;G snv 1
rs147055703 1.000 0.040 X 48698902 missense variant G/A snv 1.3E-04 1.9E-05 1