Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs63750526 0.776 0.160 14 73192832 missense variant C/A snv 10
rs2272127 1.000 0.080 2 102423413 intron variant C/G snv 0.22 3