Disease: Dementia
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80356715
TARDBP
0.807 0.120 1 11016874 missense variant C/G;T snv 8.0E-06; 2.2E-04 6
rs63750512
MAPT
0.827 0.160 17 46024010 missense variant G/A;C snv 1.2E-05 6
rs901115236
CHCHD10 ; LOC107985577
0.882 0.120 22 23767531 missense variant G/A;T snv 1.5E-05; 1.5E-05 3
rs121909334
VCP
0.752 0.200 9 35065255 missense variant C/T snv 1.6E-05 10
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs63750756
MAPT
0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs367543041
TARDBP
0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs201258663
LOC105375056 ; TREM2
0.807 0.320 6 41161457 missense variant G/A snv 5.6E-05 4.9E-05 6
rs63750959
MAPT
0.827 0.200 17 45962351 missense variant G/A;T snv 6.0E-05 5
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs63750066
APP
0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 9