Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 13
rs63751287
PSEN1
0.742 0.120 14 73192792 missense variant A/G;T snv 13
rs2200733 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 12
rs242557
MAPT
0.752 0.200 17 45942346 intron variant G/A snv 0.36 12
rs121909330
VCP
0.752 0.200 9 35065364 missense variant G/A;C;T snv 11
rs121918100
TTR
0.827 0.160 18 31595184 missense variant T/C snv 11
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 11
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs17070145
WWC1
0.790 0.120 5 168418786 intron variant C/T snv 0.43 10
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs267606673
ATP7A ; PGK1
0.776 0.240 X 78029314 missense variant C/T snv 9
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs387906709
UBQLN2
0.776 0.120 X 56565363 missense variant C/A;T snv 9
rs17518584
CADM2
0.827 0.160 3 85555773 intron variant C/T snv 0.50 8
rs63749855
MAPT
0.790 0.200 17 46014271 missense variant T/G snv 8
rs63750570
MAPT
0.827 0.120 17 46018629 missense variant G/A snv 8
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 8
rs74315413
PRNP
0.807 0.160 20 4699780 missense variant A/G snv 8
rs11931074
SNCA ; LOC105377329
0.851 0.080 4 89718364 intron variant G/A;C;T snv 7
rs63750376
MAPT
0.827 0.120 17 45996657 missense variant G/T snv 7
rs63750802
PSEN1
0.851 0.080 14 73219144 missense variant T/G snv 7
rs63751032
PSEN1
0.851 0.080 14 73219156 missense variant T/A;G snv 7
rs63751037
PSEN1
0.790 0.080 14 73173642 missense variant A/G snv 7
rs193922916
APP
0.827 0.080 21 25897619 missense variant G/A;C snv 6