Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
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
rs2695121 0.716 0.280 19 50377484 5 prime UTR variant T/C snv 0.70 16
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 13
rs6330 0.763 0.240 1 115286692 missense variant G/A snv 0.37 0.36 12
rs11669576 0.851 0.160 19 11111624 missense variant G/A snv 4.3E-02 8.4E-02 6
rs1401663578
ACE
0.882 0.120 17 63483037 missense variant A/G snv 1.4E-05 4