Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs17125721
PSEN1
0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs113993970
HTRA1
0.925 0.240 10 122506817 stop gained C/T snv 8.0E-06 3.5E-05 5
rs63749835
PSEN1
0.851 0.080 14 73192799 missense variant T/C snv 5
rs139108915
PAX5
0.925 0.120 9 36840599 missense variant G/A snv 1.0E-05 9.8E-05 3