Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs727502818 0.790 0.160 11 17772053 missense variant G/A snv 26
rs3219489 0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs148881970 0.724 0.360 17 42543840 missense variant A/G snv 5.4E-05 1.3E-04 22
rs375752214 0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 22
rs1555939456 0.851 0.200 X 20187956 missense variant T/C snv 21
rs267606959 0.732 0.200 15 89318986 missense variant G/A snv 2.0E-05 19
rs63750215 0.701 0.240 1 226885603 missense variant A/T snv 19
rs2230288
GBA
0.776 0.160 1 155236376 missense variant C/T snv 1.0E-02 1.0E-02 18
rs63751438 0.776 0.120 17 46010388 missense variant C/T snv 16
rs80265967 0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03 16
rs17125721 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs63751287 0.742 0.120 14 73192792 missense variant A/G;T snv 13
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs2072446 0.776 0.160 17 49510457 missense variant C/T snv 5.2E-02 4.1E-02 11
rs398122403 0.807 0.080 21 32695106 missense variant C/T snv 1.2E-05 11
rs63750522 0.827 0.120 14 73173644 missense variant G/A;C snv 8
rs63750847
APP
0.790 0.120 21 25897620 missense variant C/T snv 4.5E-04 3.0E-04 8
rs121912433 0.827 0.120 21 31663841 missense variant G/A snv 4.0E-06 7
rs146170087 0.925 0.040 19 29702747 missense variant T/C snv 2.3E-03 1.1E-03 7
rs3219484 0.807 0.160 1 45334484 missense variant C/A;T snv 4.8E-02 4.8E-02 7
rs515726205 0.882 0.040 19 29702966 missense variant C/T snv 2.4E-05 1.4E-05 7