Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs1554317002 0.724 0.440 7 39950821 frameshift variant C/- delins 45
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs63750424 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17