Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs367543041
TARDBP
0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs387906789
VCP
0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 14
rs652438
MMP12
0.716 0.400 11 102865911 missense variant T/C;G snv 7.1E-02; 2.5E-04 14
rs104893875
SNCA
0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs63750082
PSEN1
0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 13
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
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
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs121909334
VCP
0.752 0.200 9 35065255 missense variant C/T snv 1.6E-05 10
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs6688832
H6PD
0.752 0.440 1 9263851 missense variant G/A;C snv 0.28; 1.2E-04 10
rs767543900
MAPT
0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
rs137852642
NOTCH3
0.827 0.200 19 15192242 missense variant G/A;T snv 4.5E-06; 4.5E-06 9
rs267606673
ATP7A ; PGK1
0.776 0.240 X 78029314 missense variant C/T snv 9
rs387906709
UBQLN2
0.776 0.120 X 56565363 missense variant C/A;T snv 9
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60 8
rs63749824
PSEN1
0.776 0.120 14 73170945 missense variant C/G;T snv 4.0E-06; 1.2E-05 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