Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs74315401
PRNP
0.683 0.320 20 4699525 missense variant C/T snv 32
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs63750306
PSEN1
0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs63751287
PSEN1
0.742 0.120 14 73192792 missense variant A/G;T snv 13
rs74315452
SOD1
0.732 0.160 21 31667356 missense variant T/C snv 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
rs63750526
PSEN1
0.776 0.160 14 73192832 missense variant C/A snv 10
rs63750590
PSEN1
0.790 0.120 14 73186860 missense variant A/G snv 10
rs1386984902
APP
0.790 0.160 21 26000095 missense variant G/A snv 9
rs387906709
UBQLN2
0.776 0.120 X 56565363 missense variant C/A;T snv 9
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
rs63750376
MAPT
0.827 0.120 17 45996657 missense variant G/T snv 7
rs63750416
MAPT
0.851 0.120 17 46010373 missense variant A/C snv 7
rs63751068
PSEN1
0.827 0.120 14 73186920 missense variant G/C;T snv 6
rs63751223
PSEN1
0.807 0.160 14 73219161 missense variant G/C snv 6
rs63751278
PSEN1
0.827 0.120 14 73173631 missense variant A/G snv 6
rs121909331
VCP
0.851 0.200 9 35064167 missense variant G/T snv 5