Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs1044396
CHRNA4
0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs1805054
HTR6
0.708 0.200 1 19666020 synonymous variant C/T snv 0.15; 8.0E-06 0.16 17
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 16
rs2695121
NR1H2
0.716 0.280 19 50377484 5 prime UTR variant T/C snv 0.70 16
rs74315407
PRNP
0.732 0.240 20 4699848 missense variant G/A snv 8.0E-06 2.1E-05 15
rs367543041
TARDBP
0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs652438
MMP12
0.716 0.400 11 102865911 missense variant T/C;G snv 7.1E-02; 2.5E-04 14
rs17125721
PSEN1
0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs387906789
VCP
0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 14
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 13
rs74315409
PRNP
0.742 0.240 20 4699915 missense variant T/G snv 6.0E-05 2.1E-05 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
rs63751287
PSEN1
0.742 0.120 14 73192792 missense variant A/G;T snv 13
rs104893875
SNCA
0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 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
rs6330
NGF ; NGF-AS1
0.763 0.240 1 115286692 missense variant G/A snv 0.37 0.36 12
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 11
rs121918100
TTR
0.827 0.160 18 31595184 missense variant T/C snv 11