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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs63750756 0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs148881970 0.724 0.360 17 42543840 missense variant A/G snv 5.4E-05 1.3E-04 22
rs555145190 0.732 0.360 17 42543921 stop gained G/A;C;T snv 4.2E-06 21
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs63750215 0.701 0.240 1 226885603 missense variant A/T snv 19
rs63751438 0.776 0.120 17 46010388 missense variant C/T snv 16
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11