Disease: Dementia
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63749855
MAPT
0.790 0.200 17 46014271 missense variant T/G snv 8
rs63750756
MAPT
0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs63750959
MAPT
0.827 0.200 17 45962351 missense variant G/A;T snv 6.0E-05 5
rs63750215
PSEN2
0.701 0.240 1 226885603 missense variant A/T snv 19
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 16
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs201258663
LOC105375056 ; TREM2
0.807 0.320 6 41161457 missense variant G/A snv 5.6E-05 4.9E-05 6
rs74315401
PRNP
0.683 0.320 20 4699525 missense variant C/T snv 32
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28