Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 13
rs74315409 0.742 0.240 20 4699915 missense variant T/G snv 6.0E-05 2.1E-05 13