Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs5743836 0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs397518423 0.790 0.240 1 9726972 missense variant G/A snv 10
rs63750250 0.807 0.280 7 5986933 frameshift variant -/T delins 1.6E-05 4.2E-05 9
rs1057519953 0.807 0.200 3 49375576 missense variant C/A;T snv 8
rs267608150 0.851 0.320 7 5997388 stop gained AGGGGG/CTTCACAAC;CTTCACACACA;NNNNNNNNNNN delins 7
rs146054764 0.882 0.160 1 15506000 missense variant T/G snv 1.4E-03; 8.0E-06 1.4E-03 4
rs747141352 0.882 0.160 8 127736607 missense variant G/A;C snv 8.0E-06 3
rs923910999 0.882 0.160 20 63667537 missense variant A/G snv 4.0E-06 3
rs121918683 1.000 0.160 8 127738519 missense variant A/C snv 2
rs28933407 1.000 0.160 8 127738431 missense variant C/T snv 2
rs121918685 1.000 0.160 8 127738437 missense variant C/G snv 1