Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs74315401
PRNP
0.683 0.320 20 4699525 missense variant C/T snv 32
rs63750306
PSEN1
0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs143624519
MAPT
0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs63750756
MAPT
0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs387906789
VCP
0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 14
rs3173615
TMEM106B
0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 12
rs121909329
VCP
0.763 0.200 9 35065363 missense variant C/A;G;T snv 11
rs121909330
VCP
0.752 0.200 9 35065364 missense variant G/A;C;T snv 11
rs63749855
MAPT
0.790 0.200 17 46014271 missense variant T/G snv 8
rs121909331
VCP
0.851 0.200 9 35064167 missense variant G/T snv 5
rs63750349
MAPT
0.851 0.200 17 45996638 missense variant C/G;T snv 4.0E-06 5
rs63750959
MAPT
0.827 0.200 17 45962351 missense variant G/A;T snv 6.0E-05 5
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs74315452
SOD1
0.732 0.160 21 31667356 missense variant T/C snv 12
rs63750526
PSEN1
0.776 0.160 14 73192832 missense variant C/A snv 10
rs1386984902
APP
0.790 0.160 21 26000095 missense variant G/A snv 9
rs63750066
APP
0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 9
rs63750900
PSEN1
0.763 0.160 14 73198067 missense variant G/A snv 4.0E-06 7.0E-06 9