Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs74315401 0.683 0.320 20 4699525 missense variant C/T snv 32
rs63750424 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs63750756 0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs63750231 0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs5848 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs143624519 0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs63750306 0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs63751438 0.776 0.120 17 46010388 missense variant C/T snv 16
rs387906789
VCP
0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 14
rs63750082 0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 13
rs63750083 0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs63751287 0.742 0.120 14 73192792 missense variant A/G;T snv 13
rs74315452 0.732 0.160 21 31667356 missense variant T/C snv 12
rs80356726 0.763 0.120 1 11022352 splice acceptor variant G/A snv 4.0E-06 12
rs3173615 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 12
rs121909329
VCP
0.763 0.200 9 35065363 missense variant C/A;G;T snv 11
rs121909330
VCP
0.752 0.200 9 35065364 missense variant G/A;C;T snv 11
rs767543900 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
rs63750526 0.776 0.160 14 73192832 missense variant C/A snv 10
rs63750590 0.790 0.120 14 73186860 missense variant A/G snv 10